Regulatory And Scientific Research

Regulatory and scientific research enables our clients to comply with the organisations’ requirements for product acceptance worldwide

Regulatory And Scientific Research

Expertise, Intelligence, Strategy, And Delivery

Food Research Lab offers the unrivalled scientific, regulatory, and operational experience you require and a worldwide reach to assist you in getting your product approved for regulatory approval and market access. Regulatory development, licensing, life-cycle management, regulatory strategy input, and full-service regulatory partnerships are some of our strategic regulatory services’ activities and technical functions. To assure the quality of service, we use process improvement strategies and cutting-edge technology.
Because of the recent upheaval produced by the COVID-19 pandemic, many international regulatory bodies have published guidelines that allow clinical trials to be more flexible. Guires continues to acquire information from different agencies and update regulatory intelligence daily, both at the study level and on a country-by-country basis, to guarantee consistent compliance with regulatory revisions.

Food Research Lab can be the right fit for your Regulatory And Scientific Research.

You may benefit from our experience in successfully preparing and managing regulatory filings across the globe. We use and communicate clear, complete regulatory intelligence that is layered and verified with our current, substantial expertise.

  • Processes, deadlines, and legislation/regulations
  • Practices in the industry
  • Differences across countries and regions
  • Analyses of regulations
  • Priority in the regulatory system
  • Guidelines/directives
  • Opinions/advice

Our regulatory professionals are among the best in the business, with considerable expertise in global product development and global regulatory strategies throughout all stages and across many pharmaceutical and medical device platforms. We provide flexible, complete consulting and delivery services globally, including well-established and skilled teams.

  • Clinical trial design and implementation
  • Authorization strategy and applications for marketing
  • Management of publications and submissions
  • Control of the entire life cycle
  • Agency contacts, including complete administration of official agency meetings in preclinical consultation
  • Intelligence and strategic consultancy
  • Nonclinical expertise across a wide range of therapeutic domains
  • Expert group leadership in hot areas, including innovative therapeutics, paediatrics, and medical devices
  • Chemical pharmaceuticals, biologicals/biosimilars, medical devices, drug/device combo goods, generics, and consumer products are all areas of expertise.
  • Medical writing and pharmacovigilance are two of our responsibilities with a close working relationship.

Our worldwide presence enables us to apply up-to-date, reliable regulatory knowledge to important countries' product development and registration plans. We provide proactive solutions for anticipated regulatory roadblocks and assure the quality of filings to international organizations to increase the chances of a positive outcome.

Our country network provides appropriate regulatory representation, response, and action to support ppd and our clients worldwide.

Key contact

For further information or prices please contact us: