Automation in Medical Writing

Elevate your medical writing with Freyr's Automation Services, our integrated tools and robust quality assurance ensure regulatory compliance, optimized documentation, and streamlined processes for enhanced productivity.

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Automation in Medical Writing - Overview

At Freyr, automation in medical writing, compliant with global standards, has been designed to streamline processes and ensure adherence to regulatory standards. We utilize automation at various project milestones to save time and reduce the potential for errors. By leveraging natural language processing (NLP) and machine learning models, we ensure that documents are clear, concise, and presented in a format that meets regulatory requirements.

Our team of skilled medical writers closely supervises automated tools to ensure the accuracy and quality of the information. This approach allows us to maintain the integrity and quality of medical documentation while benefiting from the efficiency gains of automation. Our service portfolio under medical writing automation includes:

  • Narrative Writing Tool
  • Literature Review Tool
  • Formatting Tool
  • Quality Review Tool
  • End-to-End Medical Writing

Automation in Medical Writing

  • First-hand experience in advanced Tool Integration
  • Proficiency in Statistical Analysis Software
  • Effective Translation Management Systems Implementation
  • Robust Version Control Systems
  • Continuous Improvement Initiatives
  • Comprehensive Integration of Tools
  • Streamlined and resource-saving processes
  • Enhanced Quality Assurance
  • Optimized Translation Management
  • Proactive Regulatory Compliance

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​