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Fast, Reliable Gene‑to‑Clinic Development
Bring your biologic program to life with an end‑to‑end CRADS platform
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Insights Hub
Resources
Whitepapers, technical guides, and downloadable references from Vimta.
Resource
ICH M10 Bioanalytical Method Validation Checklist
Step-by-step method validation checklist aligned with the revised ICH M10 guidance — ready for sponsor and internal QA review.
Resource
EMI/EMC Pre-Compliance Testing for Medical Devices
What to test before you commit to full CDSCO certification rounds — a design-phase checklist for R&D and regulatory teams.
Brochures
Vimta Labs Capability Brochure 2026
An overview of services, accreditations, and sector specialisations across Vimta's five testing and research divisions.
White Papers
Building a Data-Integrity-First Lab: A Leader’s Checklist
21 CFR Part 11, ALCOA+, and the operational practices that make data integrity an everyday discipline, not an audit-week scramble.
Resource
Food Contaminant Testing Panel Reference Sheet
MRL reference tables for key export markets (EU, US, Japan) across pesticides, heavy metals, and mycotoxins — updated for 2026.
Resource
GLP Audit Readiness Playbook
A QA manager's playbook for preparing facility, archive, and team for USFDA and OECD GLP inspections.
Resource
Ecotoxicology Study Design Primer
Choosing the right battery of OECD ecotox studies for agrochemical and industrial chemical dossiers.
Resource
The Definitive Guide to GLP-Compliant Stability Testing PDF, opens in a new tab
A practical handbook covering protocol design, ICH Q1A(R2) requirements, sample handling, and common audit findings — distilled from 25 years of Vimta lab experience.
