How We Do It

Our major objective is ensuring success for our clients and their teams.

We acheive this by providing resources and teams of key strategists and subject matter experts and staff who are recognized for their abilities to achieve results in life science industries.

PharmaBio Staffing is committed to achieving the goal of satisfying both the client and the candidate. This is done with our attention to detail, an extensive database of a carefully screened talent pool, and expert guidance every step of the way.

Managing current federal and state regulations to ensure your pharmaceutical product is compliant with existing agency requirements within all your departments is a critical, complex and challenging process. The pharmaceutical industry is a knowledge based business, and one of its most important resources is skilled, knowledgeable people.

Whether you are searching for advice on setting up a clinical site to submitting an Investigational Drug Application or New Drug Application, creating new manufacturing suites or addressing post-marketing requirements, we work to help you achieve your goals within your timeline.

Today’s Biotechnology products and companies are a significant sector of today’s Life Sciences market. Many product challenges include IP, Manufacturing, and complex compliance regulations, to name a few.

Whether you are searching for advice on setting up a clinical site to submitting a Biological Investigational Drug Application or Biological New Drug Application, creating new manufacturing suites or addressing post-marketing requirements, we can help you achieve the goals within your timeline with the necessary talent.

The developed products created by the Generic industry must meet the same quality standard as brand name products. They must have the same efficacy versus the designated reference product, which is subsequently achieved through bioequivalency studies. In addition to this the facilities required to manage generic products must also meet the same cGMP requirements as brand name products.

New requirements for biosimilars or Follow-on biologics increases the required knowledge of staff employed to fulfill each organizations generic product objectives.

Developing medical devices requires skilled personnel who understand all the current compliance requirements for developing your products. Our team at PharmaBio Staffing is dedicated to providing you the skilled people you require to support all of your recruitment needs within each of your departments.

Whether you are searching for advice on developing a Premarket Notification 510k, or Premarket Approval (PMA) or setting up manufacturing suites or performing clinical trials, we can help you achieve your goals within your timeline.