• The developed products created by the Generic industry must meet the same quality standard as brand name products and 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. Additionally, new requirements for biosimilars or Follow-on biologics increases the required knowledge of staff employed to fulfill each organizations generic product objectives.
  • The generic industry is a knowledge based business, and that means one of its most important resources is skilled, knowledgeable people. 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.
  • We will provide you a staffing plan for each of your products and work with you to ensure that you are adequately resourced throughout your product development process.
  • Our experienced team strives to understand your current corporate timelines and challenges within your organization, and then subsequently matches your requirements with the skilled personnel necessary to achieve your product development goals.
  • Whether you are searching for advice on developing an ANDA or setting up manufacturing suites or performing Bioequivalence or preparing to manufacture Biosimilar products, we can help you achieve your goals within your timeline.
  • We have access to experienced Permanent,Contract and Consulting personnel at all levels within Clinical, Chemistry, Manufacturing, Quality, Nonclinical, Regulatory and Commercial.
  • Contact us and find out how PharmaBio Staffing can Deliver Results with Quality people.