Quality Assurance: We’ll lead the way or join the team.
When a biopharmaceutical, medical device or diagnostics company needs a QA consultant, it’s usually for one of two reasons. Either they need someone who can provide high-level leadership and guidance in establishing the company’s QA practices from the ground up or they need someone who can step in to supplement existing staff during busy times. At Complya, we address both types of needs. Our roster of consultants ranges from strong mid-level talent to some of the highest skilled, senior-level talent in the industry. Our goal: match your needs with the right person for the job.
Complya’s GxP services:
- Develop phase appropriate Quality System
- Gap Analysis and Remediation and Implementation
- Pre-Approval Inspection Readiness (Mock PAI Audit)
- Warning Letter and Consent Decree Remediation
- Batch Record and Validation Review
- GMP Training
- Supplier and Internal Audits
- Deviation and CAPA Remediation
- SOP Generation
- Document Control
- Interim support (Junior through Senior level roles)