Service Provider · +2 more types
Products: D.AI.M.I.
“PLG provides flexible Quality Support for Manufacturing Services, combining Qualified Person (QP), Responsible Person (RP), GMP, and Quality Management expertise to help…”Source: plglifesciences.com
Also offers: Regulatory Development Strategy & Agency Interactions, End-to-End Pharmacovigilance Outsourcing, +6 more
Consulting / Advisory Firm · +1 more type
“cGMP/ cGLP, cGCP Assessments including general cGMP inspection readiness, PAI readiness, facility and equipment design, PART 11 compliance as well as data integrity assessments…”Source: tunnellconsulting.com
Also offers: GxP Compliance Consulting, Technology Transfer, Process Characterization & PPQ, +2 more
CRO / Research Services Provider · +2 more types
Products: InStat, CoAuthor
“Post-inspection response drafting: FDA 483 responses, GMP non-compliance statements, Swissmedic conditions, EMA inspection responses, and structured CAPA plan development”Source: veristat.com
Also offers: Biostatistics & Statistical Programming, Full-Service Clinical Trial Execution (CRO Services), +3 more
| Vendor | Delivery model | Also offers | In their words |
|---|---|---|---|
| ProductLife Group | Service Provider | Quality Risk Management, GxP Compliance Consulting, GCP & Clinical Quality Compliance, QP Services & Batch Certification | “GDP compliance consulting, warehouse operations support, and distribution quality management expertise GMP compliance consulting and Manufacturing & Import…”plglifesciences.com · reviewed Oct 27, 2026 |
| Tunnell Consulting | Consulting / Advisory Firm | Quality Risk Management, GxP Compliance Consulting, GCP & Clinical Quality Compliance | “cGMP/ cGLP, cGCP Assessments including general cGMP inspection readiness, PAI readiness, facility and equipment design, PART 11 compliance as well as data…”tunnellconsulting.com · reviewed Oct 21, 2026 |
| Veristat | CRO / Research Services Provider | Quality Risk Management, Complaint Handling & Nonconformance Management, GxP Compliance Consulting, GCP & Clinical Quality Compliance, QP Services & Batch Certification | “Post-inspection response drafting: FDA 483 responses, GMP non-compliance statements, Swissmedic conditions, EMA inspection responses, and structured CAPA plan…”veristat.com · reviewed Oct 21, 2026 |