Quality & Regulatory

GMP Compliance

Every product that carries the Wimits name is manufactured under Good Manufacturing Practice (GMP) — the set of controls that govern facilities, equipment, personnel, and processes to ensure consistent quality, safety, and efficacy in every batch.

Our Quality Policy

Wimits Pharmaceuticals (Pvt.) Ltd. is committed to manufacturing pharmaceutical, nutraceutical, and veterinary health products that consistently meet the quality, safety, and efficacy standards required by regulatory authorities and expected by healthcare professionals and patients. We achieve this through continuous investment in our people, our facilities, and our quality management systems — treating compliance not as a checkbox, but as the foundation of every batch we release.

Certifications & Licenses

Our manufacturing facility operates under the licenses and certifications below. Certificate numbers and validity dates are placeholders — replace with your actual documentation.

License No. XXXXX

DRAP GMP License

Drug Regulatory Authority of Pakistan — Good Manufacturing Practice license for the manufacture of pharmaceutical products. Valid through [date].

Certificate No. XXXXX

ISO 9001:2015

Quality Management System certification covering design, manufacture, and distribution of our product range. Valid through [date].

Registration No. XXXXX

WHO-GMP Compliance

Manufacturing practices aligned with World Health Organization Good Manufacturing Practice guidelines for pharmaceutical production.

Registration No. XXXXX

Veterinary Health Registration

Licensed for the manufacture of veterinary health products under the applicable livestock/animal health regulatory body.

Placeholder — swap in your real license/certificate numbers, issuing authority names, and validity dates once available. Happy to add scanned certificate PDFs as downloadable links here too.

Manufacturing Standards

Our facility follows a structured, documented approach at every stage of production — from raw material intake to finished-goods release.

Our Quality Control Process

Every batch passes through a defined sequence of checks before it's released for distribution.

1

Raw Material Testing

Incoming materials are quarantined and tested against approved specifications before entering production.

2

In-Process Monitoring

Critical parameters are checked at each manufacturing stage to catch deviations early.

3

Finished Product Testing

Every batch is tested in our QA/QC lab against pharmacopeial and in-house specifications.

4

Batch Release

Only batches that pass every check are approved for release and distribution.

Regulatory Compliance

Wimits Pharmaceuticals operates under the oversight of the Drug Regulatory Authority of Pakistan (DRAP) and complies with all applicable national pharmaceutical, nutraceutical, and veterinary health regulations. Our products, facilities, and processes are subject to periodic inspection and audit to confirm ongoing GMP compliance. For product-specific registration numbers, certificates of analysis, or regulatory documentation, please contact us.