Business Process Optimization

Our Business Process Optimization (BPO) for end-to-end medical writing activities focuses on refining clinical trial processes to enhance operational performance, expedite Regulatory submissions, and ensure high-quality outcomes.

Business Process Optimization - Overview

Our Business Process Optimization (BPO) for end-to-end medical writing activities focuses on refining clinical trial processes to enhance operational performance, expedite Regulatory submissions, and ensure high-quality outcomes.

Our medical writing expert team supports you with end-to-end medical writing activities ensuring high-quality standard content for Regulatory submissions. The consultation and strategy support provided help you to optimize your medical writing domain business processes with cost-effective solutions. The team guides you at every stage of the submission project to have well-developed scientifically accurate dossier content.

Protocol development services are provided with inputs on comprehensive and accurate clinical trial designs. Our expert team provides clinical and nonclinical inputs with an effort to have minimal protocol amendments ensuring protocol optimization and overall cost savings.

The point automation initiatives within Freyr for medical writing services helps us to expedite the end-to-end medical writing solutions with high quality standards and cost-effectiveness.

Business Process Optimization - Advantages

  • Streamlined processes lead to faster project completion and reduced time-to-market for new drugs
  • Optimized processes reduce unnecessary expenditures and improve resource utilization
  • Enhances the quality of clinical data, leading to more robust Regulatory submissions
Business Process Optimization

Celebrating Customers Success

 

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

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

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​