Clinical and Nonclinical Consulting and Strategic Services

Our Clinical and Nonclinical Consulting & Strategic Services, deliver precision and compliance in regulatory endeavors. With expert guidance on nonclinical development strategy, GLP audits, and responses to regulatory queries, partnering with us assures seamless regulatory success.

For Regulatory Success, Contact Now!

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Clinical and Nonclinical Consulting and Strategic Services- Overview

Freyr believes in steadfast commitment to precision, compliance, and innovation. We specialize in providing tailored medical writing consultation to global pharmaceutical, biotechnology, and medical device companies worldwide. 

A dynamic and rapidly evolving regulatory environment necessitates consultation; that is where we come in. At Freyr, we understand the intricacies of the regulatory journey and offer comprehensive support at every stage of the process.

With a wealth of experience and a deep understanding of regulatory guidelines, our team of seasoned consultants is well-equipped to address clientele needs and help them achieve objectives confidently.

Choose us as your preferred consulting partner and embark on a journey to elevate your regulatory endeavors:

Nonclinical Consulting & Strategic Services

Landing Page with some introductory content and following list (up to 3 paragraphs) & Freyr Advantages & Expertise

  • Nonclinical Development Strategy for Regulatory Submissions
  • Consultation on Nonclinical Issues in the Submissions
  • Consultation and Responses to Regulatory Queries related to Nonclinical
  • GLP Audits of Test Facilities
  • CRO Identification and Qualification for Nonclinical Regulatory Studies

Clinical and Nonclinical Consulting and Strategic Services

  • Regulatory Documentation Expertise
  • Prompt scientific Communication Skills
  • Efficient Risk Management and Safety Reporting
  • Client-Centric Approach: 
  • Up-to-date workforce training initiatives
  • Strategic Clinical/ Non-clinical consultations
  • GxP-compliant writing capabilities
  • Leveraging Business Process Optimization Capabilities
  • Evidence-based Data Management and Analysis
  • Cutting-edge Regulatory strategic advisory capabilities

Partnering with Leading Organizations

 

Medicinal Products

Medical Writing

India

A big thanks to the Freyr team for the support they have provided to us on priority. We really appreciate the extra effort that the Freyr team has put into providing the reports on time. We are looking forward to a continuous business association with Freyr.​

Head of Quality Assurance​

India-based, Leading Pharma Contract Manufacturing Organization​

 

Medicinal Products

Medical Writing

India

A big thanks to Freyr team for the support they have provided to us on priority. We really appreciate the extra effort that the Freyr team has put into providing the reports on time. We are looking forward for a continuous business association with Freyr.

Head of Quality Assurance

 

Medicinal Products

Medical Writing

UK

We are extremely happy to inform you that the BLA was successfully submitted to the FDA. We convey our sincere gratitude to the Freyr team, who worked diligently, tirelessly, and very closely with our Bridgewater and Beijing teams over the past several months to accomplish this monumental feat on time. Freyr’s team went beyond the call of duty to make this BLA submission come true. We truly appreciate Freyr’s flexibility and eagerness to work with us to accomplish aggressive goals. Look forward to your perennial support and our continued relationship and beyond. ​

Global CMC Technical Lead​

China-based, Leading Innovator Pharmaceutical Company​

 

Medicinal Products

Medical Writing

USA

Thank you, Freyr team. I appreciate your professionalism, dedication, and hard work. You’ve gone above and beyond to ensure all deliverables were met ahead of schedule throughout the project and have done a great job managing a challenging group of products. I appreciate your attention to detail and follow-up on the large workload you’ve managed. It’s been a pleasure working with you, and I wish you and your family all the best in the future!​

Director, Global Labeling Management – Labeling Cluster Head Global Product ​ Development, Global Regulatory Affairs

US-based, Multinational Pharmaceutical and Biotechnology Company​

 

Medicinal Products

Medical Writing

Vietnam​

Thank you so much for being a great partner in our Regulatory compliance journey.

As Asian countries move towards having safety assessments as a key requirement, your support has helped us significantly in fulfilling those requirements well ahead of our competitors in Vietnam. ​

In fact, I shared your contact with our regulatory officers so that they can share it across the industry if the safety assessments become necessary.

Lead, R&D/Personal Care

India-based, Multinational Consumer Goods Company​

 

Medicinal Products

Medical Writing

USA

Kudos to you all for the brilliant teamwork !! Alone, we can do so little; together, we can do so much.

Look forward to the next milestone and collaboration on new projects in the future.

SVP - R&D ( Finished Dosage Form)​

US-based, CRO Company that Focuses on Material Science and Engineering for Drug Development​