Non-Clinical Regulatory Submissions
A wealth of expertise supporting the submission of non-clinical documentation
Non-Clinical Regulatory Submissions
A wealth of expertise supporting the submission of non-clinical documentation
Decades of experience in authoring Non-Clinical Regulatory submissions
At G&L, we have a wealth of experience supporting the successful delivery of non-clinical regulatory documents.
Our seasoned team specializes in authoring the non-clinical components of regulatory submissions. With meticulous attention to detail and a deep understanding of regulatory requirements, we ensure that your documents are clear, compelling, and fully compliant.
Partner with us to streamline the submission process and bring your therapies one step closer to market.
Services include:
- Authoring of non-clinical content of: INDs, CTAs, IMPDs, IBs, briefing books, MAAs/NDAs/BLAs etc.
- Specialist toxicology and pharmacology expertise
