Pharma Pro Services

Integrated Solutions to Advance Innovations

Clinical research services are all about accelerating and smoothening the process of drug or device development. So, a CRO must satisfy the broad spectrum requirements of clinical research including clinical, compliance and regulatory services. Pharma Pro Services offers all these and more with a focus to ensure high quality, efficient and timely completion of the critical research.

Research

Our plan of action starts with thorough research about the client and its requirementsin terms of their clinical research.

Develop

Followed by research, our team of experts develop strategies to fast track the process of your innovation.

Deliver

With our expert team and wide range of solutions, we are accomplished to deliver-every service to our client.

Support

Our always available and ready to help support team not only works during the project, but even after project completion

Comprehensive Clinical Research Services

Acting through a wide range of services for pharmaceutical, Biotech and medical device companies, our comprehensive solutions will confidently navigate you through all the hurdles for successful completion of your research.

Medical Writing

Medical writing is a pivotal part of clinical research and drug development. A well-developed medical or regulatory document strengthens the research while an under-developed document can ruin the efforts of years long research.

Drug Safety and PV

In clinical research, it is must to recognise the crucial information about your product safety on time. Our drug and pharmacovigilance consultants work with client's team to prepare regulatory ready reports for pre-clinical, clinical as well as post-marketing concerns.

Data Management

Clinical data integrity is chief requirement for successful completion of clinical research at every stage. In addition, data that is clean and reliable can also decide the fate of a clinical trial. As every pharma company aims to market its drug as quickly as possible.

Clinical Operations

Clinical operation is undoubtedly one of the most critical aspect of clinical research. It takes a lot of efforts to finely plan and execute a clinical research while mitigating risks.Moreover, with increased regulations and guidelines, it has become progressively critical to put time and efforts.

Regulatory Affairs

The clinical journey of a new product is often difficult and lengthy. It involves preclinical development, clinical trials, regulatory submissions and finally regulatory approval to market the product. The most tedious and stringent of all these is regulatory affairs.

Publication Management

Publication is an important aspect of clinical and scientific research. It is the best way to connect, inform, and exchange knowledge within members of same community. But the process of publication is a very daunting task, especially for extremely busy research professionals.

Statistics Management

Statistical analysis is a crucial part of clinical research. It involves strategic and compliant conversion of clinical research data to knowledge so as to support the early and successful development of new medicines. With ever changing dynamics of the regulatory in clinical industry.

Lifesciences Staffing

Lifesciences is a complex stream with so many different roles for every education. This makes it often tricky for the recruitment team to find the right candidate with specific skills for clinical research and trials. We at Global Pharma Tek understand the challenge of finding right skills for specific role. Our life science staffing services.

Learn, Earn & Excel

Pharma Pro Services has opportunities for you, starting from entry level to top level positions in various lifesciences companies.

Customized Lifesciences Recruitment Solutions

If you are looking for a challenging yet satisfying opportunity, we are here to connect you with your Success.

Have a project with us? Feel free Get in Touch