Quality RA

About Quality RA

Quality RA offers CMC and RA services to biotech. & pharmaceutical companies, large and small.

A selection of our services:

- Writing or review of regulatory submissions (Modules 2.3 and 3 of CTAs/INDs, MAAs/BLAs, EU/US post-approval change submissions, scientific advice briefing documents) - CMC review and advice on regulatory strategy - Gap assessments for submission readiness - Providing advice on: comparability; justifications of specifications; development, validation and transfer of analytical procedures; setting up and reporting stability studies, reference materials - Writing or review of CMC study protocols and reports - Due diligence support - Interim CMC/QC/RA roles

Keywords

• Cmc Ra
• Cmc Writing
• Submission Co-Ordination

Address

• Headquarters

  LeidenZuid-Holland, Netherlands

Team by function

Based on 1 public job profiles as of 3 September 2026.

• Other / Unclassifiable1