Quality & Compliance

Quality, documentation & regulatory responsibility

Pharmaceutical products require careful attention to quality, documentation and market-specific regulations. We support our partners with relevant product information based on the product, manufacturing arrangement and destination-market requirements.

Quality Policy

We manufacture and export generics and best-quality branded-generic products for routine, allergic and chronic diseases in human treatment — with a dedicated veterinary division and a good range of nutritional food products.

Every formulation is matched to its purpose: allopathic ranges for human use, and veterinary formulations selected by animal and disease type.

R&D Facility

A compact R&D centre, built for precision

Designed to carry out F&D (formulation design & development) and AMD (analytical method development & validation), the facility works in two parts — lab-scale manufacturing, and testing & analysis.

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Part One

Lab-Scale Manufacturing

Equipment for orally administered products — tablets in different shapes, chewable, flavoured and taste-masked variants, plus liquid orals — with precision and accuracy.

  • Complete manufacturing set-up for 5 kg lots, fitted in an isolator for tablets
  • Weighing balance, RMG and FBD, with scoops at all required stages
  • Manual tablet compression machine
  • Manual capsule-filling sets for all sizes
  • Oral liquid syrup & suspension manufacturing set
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Part Two

Testing & Analysis

Product-testing instruments and equipment supporting analytical method development and validation — the best instruments for the job.

  • HPLC
  • HPTLC
  • AAS (Atomic Absorption Spectrophotometer)
  • Flame Photometer
  • Viscometer
  • Complete set of instruments for wet chemical testing

Documentation that may be available

Depending on the product and destination market, the following documentation may be provided. Only documents and claims that BQM Impex can genuinely provide will be issued.

  • Product specifications
  • Certificate of Analysis
  • Manufacturing licence details
  • GMP-related documentation
  • Stability information
  • Packaging specifications
  • Registration-support documents
  • Product artwork & labelling information

Market-specific availability

Product availability, pack size, formulation, artwork and documentation may differ according to regulatory requirements in the destination country. All supply is subject to applicable laws, registration requirements and commercial confirmation.

Need specific documentation for your market?

Tell us the products and destination country and our team will confirm what can be provided.