Testing and Compliance Services

Testing can easily become the bottleneck between development and approval when laboratories, protocols, and regulatory expectations are not aligned. We coordinate testing and compliance activities so your analytical, microbiological, and safety data support submissions from the outset.

Working from your regulatory objectives, we identify the right test panels and specifications for drugs, cosmetics, OTCs, and related health products. We then liaise with vetted third‑party laboratories, obtain quotations, align methods with pharmacopeial or regulatory standards, and schedule work to match filing timelines.

Throughout each project we track sample movement, monitor timelines, and review draft reports for the elements regulators expect to see, such as validation summaries, acceptance criteria, and clear conclusions. This approach reduces back‑and‑forth with laboratories and prevents late surprises, like missing stability points or incomplete preservative‑efficacy data. You benefit from data packages that integrate smoothly into your dossiers, fewer repeat tests, and a far more predictable critical path from development through regulatory review.