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Welcome to ASSAY CR

ASSAY with its global presence is a service provider of innovative and technologically advanced solutions for clinical trial management for the pharmaceutical, biotechnology and medical device industries. We also extend our services to clinical research organizations who require tailored services for managing their clinical trials. We focus on developing effective strategies for the collection, management and analysis of clinical data. With us, we guarantee that Sponsors, CROs and Sites can gain access to the best services for Phase I-IV clinical studies, study management and site management. We also ensure that the best skills and experiences are put in place to achieve the milestones efficiently. Together we can aim to achieve maximum patient safety and accurate data generation with highest quality and regulatory standards. Please have a look at the Services and technologies we can offer.

About Us

Established in the UK in the year 2012, ASSAY Clinical Research started with a group of clinical research professionals who have been providing a variety of services for the pharmaceutical industry and other clinical research organizations. Gradually, ASSAY has gained recognition for its quality, timely services with affordable costs. Our services were quickly extended to European regions and India. With the deadly outbreak of Ebola and the need to test the vaccines, ASSAY was chosen for project management, data management and monitoring services and these services in Sierra Leone.

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Global Presence
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Tailored Services
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Affordable Pricing
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Assured Quality
Tailored Services


Client satisfaction depends on delivering to the exact needs of a client. And this can be achieved only through carefully designing our services and strategies to your requirements. We at ASSAY, offer a range of tailored services to suit your needs and improve the delivery



Feasibility Studies:

Prior to deciding on the huge investment on a clinical trial, it is vital to have a market research done. Any feasibility study would provide a vital insight into:

  • 1. The disease prevalence in the selected regions
  • 2. The need for better treatment options
  • 3. The availability of potential patients / volunteers
  • 4. The interests among potential Investigators
  • 5. An insight into the regulator environment
  • 6. Specifics on timelines and budget
  • 7. And more...

At ASSAY, our experienced team will be able to conduct a feasibility study tailored to your research protocol within the shortest timelines possible as we have a strong database of information related to sites and their experiences. Within minimal time, ASSAY will be able to provide a detailed insight into the feasibility in terms of resources, patient population, regulatory timelines, budget expectations and any other technical aspects that your research is aiming for. We will provide comprehensive data in the form of tables, charts and reports for easy interpretation and quick decision making. We will be able to simultaneously conduct feasibility studies across two or more regions depending on your requirements.

Our SWAT Team

With growing number of research activities around the globe, it is increasingly essential to keep up with the quality and timelines to save potential lives and curb the budget. With ever changing dimensions of research companies and the demand for therapeutic specific experience, the challenges to find the right resources has suddenly become massive leading to a demand and supply issue. ASSAY is here to help you with this. Our experienced team of project managers, clinical research associates and in-house team will be able to understand your challenges and needs in a time efficient manner and plan out the CAPA for you and implement it at any level which may be considered appropriate (Site Level, CRO level, Sponsor level, Country level, Region level or Global)

Our team will assist and deliver:

  • 1. Study or Organization specific Process designing and implementation
  • 2. Identification of concerns (Critical, Major or Minor) at all levels
  • 3. Coordination at regional or global level for CAPA planning and implementation
  • 4. Clearing data backlogs in terms of data entry, source data verification and query resolution
  • 5. Training at site or organization level including development of training materials
  • 6. Provide comprehensive reports to the clients on the outcome
  • 7. Keep the study AUDIT READY!!


Process and SOP Development

With the growing number of clinical trials all over the globe, many small to medium sized CROs come under the pressure of undefined processes and procedures within their organization which leads to a chaotic situation affecting the overall outcome of the clinical trial. In this process, these developing organizations run the risk of losing clients and valuable business even if they have acquired and retained the required experience and expertise. ASSAY will assist struggling organizations in developing the required processes and Standard Operating Procedures based on the needs of the project or client. We will support you through the review of your processes as well and provide you with constructive suggestions towards improving the standards. This in turn will support you throughout and build the most effective relationship between yourself and the clients.

Defined and Detailed Trainings

Practically, there may be only a handful of people in an organization who actually know "what-to-do" and "when-to-do" without being told to do so. Again, many employees today are not afraid of shifting laterally into a different department, or even shifting on to a new career path altogether, in order to attain personal goals. So, it is not sufficient to simply hire an employee and assume that he has adequate knowledge. The present clinical research scenario is constantly evolving and updating itself in terms of technologies and is also rapidly changing with new rules and regulations coming up every day. In order to meet the needs of a constantly changing workplace/workforce, and of course; wanting to retain your valuable employees, it is but natural for an organization to want to have trainers who can help widen your employee's outlook and comfort level in the job and also help them grow and develop their career path. At Assay, we specialize in proving detailed and defined trainings & trainers to meet your everyday training requirements. Whether it is a single session or a series of sessions over multiple days, we will work towards the need of your organization. We are there to train your CRAs, managers, investigative sites or even your entire staff ; be it for an updated regulatory environment, a specific therapeutic area, any other study related everyday activity, soft skills trainings or even a refresher course - feel free to use/customize our services per your needs. It is often seen that an employee who feels that his company has invested in him via trainings and other similar measures, has a certain sense of pride, loyalty and better productivity than his peers and is more likely to stay invested in the company's growth. Having an in-house training department is not easy for every organization due to its huge cost and also as because it's not an everyday need. Therefore many organizations whether small or large consider purchasing prepared material or outsourcing training. Assay's trainers are well versed in training techniques and will also be cost effective.

Regulatory Consultation

A strict regulatory environment is the first challenge faced by any organization willing to conduct clinical trials in a specific country or multiple countries. Few instances also lead to the company not being able to choose a specific country only because of their lack of knowledge of the regulatory requirements or the non-availability of experienced personnel to handle the application process. ASSAY with its extensive database of researched regulatory requirements for all countries and with their experienced team in each of these countries can assist you throughout the application process.

ASSAY can assist you in:

  • 1. Consultation for the requirements for one or multiple country application
  • 2. Coordinate the submission of your application with the regulatory authorities
  • 3. Collect, Compile and Complete all the required documentation for a successful submission
  • 4. Keep you updated with the progress of the application


CRA Assessments

Practical experiences leave a lasting impact. It is no better understood by a Clinical Research Associate, whose work profile involves a variety of aspects including people management, time management, travelling etc. When CRAs are new, they are skeptical about their performance while experienced CRAs in their way to achievement and recognition become overburdened. With highest levels of multi-tasking, it is always possible to slip away from the study goals, timelines and quality. However these can be overcome by a well-structured training and assessment program specific to the employee and their experience. At ASSAY, we will assist your team by understanding their background, skills, work pattern and areas of development. This understanding will help us tailor the training and assessment program and roll-out in an effective fashion. For new or experienced CRAs, we will provide study related practical training, skills development, personality development, communication enhancement, organization skills, and people management both on study sites and off study sites. We will roll-out these programs in coordination with the study activities already planned for the CRA so that we ensure the trainings do not affect the timelines of the study. Moreover, we will continue to assess your CRAs on their performance and provide a detailed feedback report which can be used by you or your clients during performance review. For assessments which are "for-cause" and the cause is related to study, site, audit or employee, ASSAY will structure the assessment program after a thorough discussion and the assessments can be done on a site level or CRO/Sponsor level. Detailed assessment report along with recommendations and assistance for implementation will be provided.

Tailored Technologies

ASSAY is an organization which believes in being paperless to the maximum extent possible. Use of technological solutions contributes towards this goal and so ASSAY is a technology oriented company and encourages others as well to ride on the same path. However, not all organizations may have the knowledge of expertise to choose or develop such solutions. ASSAY is your solution. We at ASSAY are here to provide consultation and develop technologies for you to ensure that it serves your requirement and makes your study management easier in one or many aspects. If you choose any of our technologies and would also want to tailor it further to suit your study requirement, we are happy to consult you for this as well.

By choosing our tailored technology service, you will:

  • 1. Benefit from the use of tailored and advanced solution for effective management of your clinical trial.
  • 2. Save on time and money involved in developing and maintaining paper based or primitive management solutions
  • 3. Perform the same activities much quicker when compared to conventional methods
  • 4. Generate user-friendly reports for metrics measurement

Apart from tailoring your solutions, ASSAY will also assist you towards the maintenance and improvement of the solution.


ASSURED QUALITY

Quality, is the primary concern for any clinical professional, as the drug being tested, should prove to be safe for treatment/prevention/cure while complying with the ethical principles. Our expert auditors, not only ensure quality but also assist in enhancing the quality in a clinical trial. Our expert team of auditors will serve as an epicenter for your clinical trial and will assess every step of the trial, whether at the level of the site, or CRO or technology, or even any third party vendor. Our team of experts is experienced in conducting audits in various regions under different regulations including the FDA, MHRA, EMEA and DCGI following GCP, GLP and GMP guidelines. Our compliance with regulations ensures that our clinical trials are also compliant. We will excel for achieving excellence.

AFFORDABLE PRICING

Clinical trials in its various processes for testing new drugs also opens a window for patients to try new treatment options for their diseases / aliments and this treatment is always provided of no charge. This gives an opportunity for patients to relieve themselves from the financial burden of their treatment. We believe that the conduct of clinical trials should also be affordable to our clients so that they are able to get new treatments into the market in a more effective, efficient and competitive pricing model. Making our services affordable for you will ensure that you are able to distribute your costs in various other activities in the drug development process. Our pricing will support you throughout the conduct of the trial with the highest quality standards. Please contact us to know more about what we cost.

OUR SERVICES


PHASE I - IV

We understand that that a molecule, at the start of its journey, requires the most attention to make it into a potential life saver drug in the future. With our expertise in handling various types of studies,experience in a wide range of therapeutic area, our ability to handle different dosage forms and complicated protocols enables us See more.


Our therapeutic expertise is across:
1. Oncology
2. Cardiovascular
3. Rheumatology
4. Rare diseases
5. Gasteroentrology
6. Infectious diseases
7. Vaccine studies
8. Pain management
9. Pediatrics
10.Central Nervous System and many more.
It is our responsibility to ensure that your clinical
trial is handled only by the experienced and experts.
We will excel for achieving excellence.

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ASSAY ACADEMY

The gift of knowledge shared in good faith benefits the giver as well as the receiver. Clinical Research is a specialized field of both medicine and the healthcare industry, which plays a vital part in bringing new treatment options for the patients in need. A burgeoning Clinical Research industry has proved See more.

TECHNOLOGY

The world is surrounded by a variety of technological solutions for every activity occurring on this earth. Clinical Research is no alien to technology. But the need for an improved technology is always present and ASSAY is striving towards fulfilling this need GRAVITY During an entire process of drug development, we generate vital information See more.

for a team of most experienced and trained. ASSAY will assist you through this. At ASSAY, we identify clinical monitors who are experienced in the therapeutic area and are experts in supporting the site staff and in maintain high levels of communication skills. Our extensive training programs for our monitors ensure that we are able to deliver quality performance well within the timelines and costs. Our Clinical Monitoring Services are tailor made to your needs. It can range from: Study plan development , Site and supply management , Regulatory documentation management , AE and SAE management , Source document review , Clinical Operations We will serve as a clean and transparent window which will ensure open communication and lead to the success of the clinical trial in every aspect. We will excel for achieving excellence.

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V-Share

Need the best experience for your trial, require a team of well trained and experienced individuals for your trial management or require experts to assist you with the progress and quality, our unique staffing solutions through V-Share will ensure that your requirements are achieved.



Phase I (Early Phase)

We understand that that a molecule, at the start of its journey, requires the most attention to make it into a potential life saver drug in the future. With our expertise in handling various types of studies, experience in a wide range of therapeutic area, our ability to handle different dosage forms and complicated protocols enables us to provide innovative and quality solutions to your studies. Our services for phase I trials includes designing and managing of First in man studies, Proof of concept studies, Bioavailability and Bioequivalent studies, Drug interaction studies, Dose escalation studies, safety studies and special population studies. We will be assigning a dedicated team headed by a project manager, all of whom will be experienced in handling your requirements along with the therapeutic knowledge required. The team will be accessible to you anywhere, anytime which will allow establishing good communication, robust planning and minimising risks in the most time and cost efficient manner. After all, patient safety is achieved through protocol compliance and our working model will ensure that this is achieved with highest quality standards including GLP, ICH, GCP and all other local regulatory guidelines. ASSAY with its technologies and expertise will assist you through every step of your trial.


Phase II/III

Due to the sheer size and complexity of phase II and III trials in terms of recruitment, duration of the study and the costs involved, it is important that the most experienced and trained resources are available in order to obtain the most accurate results. At ASSAY, we have the ability to get connected to the perfect resources and expertise throughout the globe which will ensure that clients / sponsors are provided customized plans to execute their clinical trials successfully within the timelines and budget and with high quality standards. We offer Clinical monitoring, Data Management, Project Management, Investigator Recruitment and site management, Protocol and CRF designing, Patient Reported Outcome management, Feasibility studies, Interactive technologies and any other customized services as required by the clients or project. ASSAY is committed to patient safety, ethics, quality and paramount client service.


Phase IV (Late Phase)

A safe journey from development to commercialization is vital to make the drug reach out to the humanity. ASSAY with its trusted partners will successfully conduct post marketing studies through our strong therapeutic expertise, good documentation and effective communication. ASSAY will strive to assist our sponsors in the post-approval process in a cost effective manner within the expected timelines.


Regulatory

Clinical Trial set-up is the first and most crucial step towards successfully conducting the trial for the given duration. With stringent regulations in every region and country and its ever changing requirements, it is important to choose the right partner to start off the regulatory submissions which will ensure that all the requirements are taken care off by the right and experienced people. At ASSAY, our team of experienced professionals who are trained and constantly updated with the regulatory requirement of each country, will be able to assist you throughout the submission process for central regulatory agencies, local regulatory authorities (country and site specific) and license management (import and export licenses) throughout the duration of the trial. Our commitment to ethical standards and adherence to regulatory guidelines will ensure that our sponsors receive the correct consultation and assistance in every step of the regulatory submission.


THERAPEUTIC AREA EXPERTISE

Irrespective of the size of the trial, it is vital to be experts in the therapeutic area of the trial which will become a strong platform on which the clinical trial can be planned and executed successfully. At ASSAY, we have teams dedicated to each therapeutic area and our specialized resources will ensure that your clinical trial is given the right attention in every aspect.
Our therapeutic expertise is across:
1. Oncology
2. Cardiovascular
3. Rheumatology
4. Rare diseases
5. Gasteroentrology
6. Infectious diseases
7. Vaccine studies
8. Pain management
9. Pediatrics
10.Central Nervous System and many more.
It is our responsibility to ensure that your clinical trial is handled only by the experienced and experts.


CLINICAL TRIAL MANAGEMENT

For complex global trials or focused regional studies in all phases, the right research partner makes all the difference in how well your trials run. Based on your specific research requirements, ASSAY assigns you an expert project manager and a dedicated team, including researchers experienced in your particular therapeutic area.


Clinical Monitoring

As soon as a protocol is finalized and ready to be introduced to potential investigators who would facilitate in conducting the trial, the clinical monitoring team gears up to be in the front line between the study site and the sponsors. Their crucial role in maintaining the safety and efficacy of the trial and to maintain ethics and quality calls for a team of most experienced and trained. ASSAY will assist you through this. At ASSAY, we identify clinical monitors who are experienced in the therapeutic area and are experts in supporting the site staff and in maintain high levels of communication skills. Our extensive training programs for our monitors ensure that we are able to deliver quality performance well within the timelines and costs. Our Clinical Monitoring Services are tailor made to your needs. It can range from: Study plan development , Site and supply management , Regulatory documentation management , AE and SAE management , Source document review , Clinical Operations We will serve as a clean and transparent window which will ensure open communication and lead to the success of the clinical trial in every aspect. We will excel for achieving excellence.

ASSAY Academy


The gift of knowledge shared in good faith benefits the giver as well as the receiver. Clinical Research is a specialized field of both medicine and the healthcare industry, which plays a vital part in bringing new treatment options for the patients in need. A burgeoning Clinical Research industry has proved its mettle to society by bringing safe and efficacious medicines and devices to market in timely cost effect manner. ASSAY Academy believes sharing of knowledge amongst Clinical Research professionals is a worthy and valuable endeavor and aspires to implement training at the highest standard. We want to implement this concept by taking knowledge and training to the next level. With clear, concise and well-structured courses, ASSAY Academy serves as a single window for any aspiring medical / science professional to educate themselves in the field of clinical research. With real-time practical information in each of the courses, along with case-studies and assessments, every individual enrolled into the courses can rest assured that they are receiving most updated and accurate information. Our experienced and expert team of trainers and clinical research professionals has assiduously designed each of the courses and their related material to ensure that the information provided is pragmatic as well academically sound. ASSAY provides easy to access online courses for a variety of healthcare professionals including Site Staff and CRO (Clinical Research Organization) personnel of all types. Assay will also provide ad hoc Instructor-Lead Training for specific topics which you might be interested in or for those areas you may require assistance with. With role-specific trainings to choose from, you can be assured that the training is tailored to your needs and your job specifications, boosting knowledge and confidence in the practical environment.

The Team

With over 25 years of experience in clinical research, our team has seen through the growth of the industry and has gained extensive knowledge and experience about the functions and processes involved in successfully conducting a clinical trial. With a combined industry experience of over 35 years across a range of therapeutic areas, countries and teams, our trainers and expertise involved in structuring of the courses, ensure that the course materials are of the highest standards and meet the industry expectations. Our aim is to provide a realistic experience of a clinical trial environment in a controlled risk-free set-up, so that individuals are confident while implementing their new knowledge in real-time. Our team will be available throughout your course for assistance and any questions which you may have, to help you get through the case-studies and assessments for a successful completion of the course. After course completion, our team will still be available to mentor you through your work environment, whenever in doubt


Course Modules and Target Audience

Whether you are an Investigator, or another member of staff from a site, or if you are a Trial Assistant, Research Associate, Trial Manager or Project Manager from the CRO or Sponsor side, we have role-specific modules for each of you. Our course modules range from general Regulatory trainings (GCP, FDA, CFR, DCGI, MHRA, EMEA etc.) to role-specific trainings. All of our courses can be found in the website. Once registered to one of the courses you are interested in, we will be able to recommend you further modules which will enhance your knowledge and experience of the practicality of clinical research. For example, when an Investigator registers for an online GCP course, we will be able to recommend course / modules like Investigator responsibilities in clinical research, FDA expectations from sites, audits and inspections in clinical research etc. You can be assured that only courses relevant to you will be suggested ensuring that you are provided with only your perspective of clinical research. Once completed, you will be provided with a course completion certificate from ASSAY and you will always have the opportunity to enroll into any of the refresher courses and stay updated.


Technology

In the era of technology, virtual training has become a preferred option. It provides

  • 1. Easy, multiple and stress free access
  • 2. Time to work through the training materials at the learners own pace
  • 3. Controlled, risk-free environment which enhances concentration
  • 4. Cost and time effective
  • 5. Interactive and fun way to gain knowledge


All our courses and training modules are provided as on-line (Web-based or Instructor-Led), easily accessible from either home or office.


Assay Gif
Our Android App which calculates the basics of clinical trials like drug compliance and visit window.

Check out our brochures to know more about each of our services and
technology...

Technologies


The world is surrounded by a variety of technological solutions for every activity occurring on this earth. Clinical Research is no alien to technology. But the need for an improved technology is always present and ASSAY is striving towards fulfilling this need



GRAVITY

During an entire process of drug development, we generate vital information on the molecule, disease and the different dimensions in which the molecule acts and reacts. All this research needs documentation and hence a lot of paperwork is generated. Managing clinical trials is a tedious task and requires the most attention for quality outcome in a time-bound manner. But equally tedious is the management of the data generated from it. The need of a robust system with user-friendly design is essential for this purpose. GRAVITY is our Electronic Trial and Site File Management System (eTMF and eSMF) which has been designed by the experience and knowledge of our project and site teams. The system ensures that:

  • 1. Documents generated during each step of the clinical trial are maintained in the appropriate manner similar to the paper filing structure.
  • 2. Documents synchronise between the central and site files across various locations which in turn ensures that documents are made available and filed in a timely manner
  • 3. All important documents and information (including safety) are available to Site, CRO staff and Sponsor in a timely manner
  • 4. Documents are managed by just few clicks
  • 5. All file reviews occur in-house which in turn ensures that the time of site monitors are best utilized on site.

GRAVITY is built for those who believe quality comes from timed perfection


PROMPT

With everything changing towards being electronic, the need for a paperless patient management system within the context of clinical trials is increasing in demand. All those who are contributing towards a clinical trial (from patient to Sponsor and vice versa) deserve a management system which gathers information and synchronizes it with just few simple buttons. PROMPT is our combined ePRO (Electronic Patient Outcome) and eCRF (Electronic Case Report Form) system which aims to the most credible data required for analysis, directly from patients. As an ePRO system, PROMPT will reach directly to patients for recording AEs, SAEs, drug intake and compliance and also will provide updated information related to the study (patient specific) in real-time. As an eCRF system, PROMPT will extract real-time information from patients and synchronize it to various user groups. Since PROMPT is a combination of ePRO and eCRF, its features and use are extensive. We have attempted to illustrate the current features of PROMPT and those which are up-coming. Also we have divided the features and uses as:

  • 1. Patient Level
  • 2. Site Level
  • 3. CRO Level
  • 4. Sponsor Level
  • 5. Others.

PROMPT can be accessed from any smart phones, tablets, laptops or desktops which have connectivity to internet/wifi or mobile data. This ensures that PROMPT will be available for you anytime, anywhere.


CliniCAL - Android App

CliniCAL is a collection of user-friendly calculators designed and validated by ASSAY. These calculators can be used by Patients, Doctors (Investigators), Nurses, Pharmacists and all other clinical and healthcare professionals who are involved in everyday management of clinical trials and/or patient treatment. The App was developed with the best of interest of all those who are involved in clinical research and healthcare sector


Strategic Resourcing - V-Share


Change is constant in this world and every change brings with it new challenges. Drug development in pharmaceutical / biotechnology / medical device industries being crucial on its own, is influenced by these changes and challenges which in turn affects the time and costs involved ,which may cast a shadow of compromise on quality. Investments involved in handling these challenges also incur a huge cost which becomes a challenge in itself. One among these challenges is resourcing. Hence, you now need a perfect partner for all your resourcing challenges, where the partner is able to offer effective solutions for staffing and managing resources based exactly on your needs. V-Share in clinical research industry will be able to out-source you an individual or a team of professionals to assist you with a part of your project or the entire project, full-time or part-time, anywhere across UK, Europe, Asia and West Africa.

Got a task/project and bothered about headcount for V-share

A key struggle faced by most organizations is spending too much time on small and routine tasks while conducting clinical trials. Compounding this problem is the cost and employee factor. V-share helps pharmaceutical / medical device / Clinical Research Organizations to overcome such challenges in a time and cost effective manner. We will be one amongst you and accomplish the tasks given to us. The tasks can range from one single activity to a combination of multiple tasks with flexible FTEs. With V-share you can hire us for a specific task where we can act as your in-house team. Or we can identify the best candidate for your project needs and also provide line management solutions to ease out your commitments. V-share is the strategic resourcing department within ASSAY Clinical Research Limited, which is a UK-based Clinical Research Organization, providing expertise consulting and business solutions for pharmaceutical / biotechnology / medical device industries and other CROs for conducting their clinical trials.



Our Flexible Resourcing Solutions:-

a) Choose an individual or a team:

With a wide range of experienced and skilled clinical research professionals to choose from, you will be able to hand pick an individual or a team based on the requirements and we will ensure that the results are delivered with high standards of quality.


b) Specialised and trained team:

Our professionals are trained, experienced and have the required expertise in conducting clinical trials. We are also experienced in a wide range of therapeutic areas which provides added advantage in understanding the project needs.


C) Line Management Solutions:

Our experienced professionals provide the best training for all your clinical operations needs like conducting site visits, performing source document verification, ICH-GCP etc. Trainings can be done both on-site and off-site, for client staff or site staff depending on your needs. If you need a specialized team to assess the progress of your study or assess an individual staff, we can provide you with our experts. People, performance and payroll management are all our responsibility, when you choose us.



Our Aim


Our aim is to deliver the client requirements in an efficacious manner by reducing costs and maintaining high quality. Our services can be used from small sized projects to multinational projects in a combined manner or on an individual basis. We provide resourcing services of reliable staffing and FSP roles and train them to suit your specific project needs.



Advantages of associating with V-share

a) Guaranteed productivity and performance:

With our professional expertise we can provide you best productivity and performance with high standards of quality. We provide weekly and monthly reports on work status so that you can track status with zero compromise in consistency and quality.



b) No long-term commitment:

With our innovative V-share you can hire an employee/a team or outsource your project only for your specific needs rather than making a long term contracts.



c) Flexibility:

Our V-Share concept offers flexibility and a complete pay-as-you-go model, where you can upgrade or downgrade your services anytime you like



d) Affordable prices:

Long term contracts and hiring for an entire project when the need is only for a particular task can incur a huge cost to the company. V-Share with its unique hiring model ensures that you get the best experienced team or individual at a very affordable cost.


Global Reach


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Contact Us






United Kingdom (Registered office)

56 Pennington,
Orton Goldhay,
Peterborough - PE2 5RB,
United Kingdom

India (Registered office)

23, Sheerin Castle, 2nd Main Road,
Alwarthirunagar Annexe,
Alwarthirunagar, Chennai -600087


Offshore Development Center

Golden Rays Building,
29A LakeView Road, West Mambalam,
Chennai - 600033

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