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Prix Pharmaceutica (Pvt) Ltd.

Science behind every standard.

Prix Pharmaceutica evaluates veterinary products through scientific assessment, controlled manufacturing, documented quality practices and responsible use.

Science

Scientific evaluation for veterinary use

Product selection and development are grounded in scientific evaluation of composition, formulation and intended veterinary use.

  • Scientific basis

    Each product is evaluated for scientific basis and suitability for veterinary animal-health use.

  • Ingredient evaluation

    Active ingredients are assessed for evidence, stability, delivery and intended veterinary use.

  • Evidence-informed guidance

    Technical support is based on current evidence, not unverified claims or unsupported product promotion.

Scientific evaluation, formulation discipline and evidence-informed veterinary guidance.

Explore our scientific approach

The team keeps current with veterinary pharmacology, animal-health science and commercial production practice so technical guidance stays relevant to field conditions.

Scientific evaluation

Science-based product evaluation backed by ingredient evidence.

Each product is evaluated for scientific basis, active ingredient evidence and suitability for veterinary animal-health use.

Formulation knowledge

Active ingredient stability, delivery and interaction insight.

Understanding of active ingredient stability, delivery and interaction guides our product recommendations.

Animal-health expertise

Focused on livestock, equine, poultry and companion animals.

Focused on livestock, equine, poultry and companion animal health requirements.

Technical literature

Technical data, package inserts and product documentation.

Products supported by technical data, package inserts and product-specific documentation.

Evidence-informed guidance

Technical support grounded in current evidence.

Technical support is based on current evidence, not unverified claims or unsupported product promotion.

Responsible product use

Stewardship, withdrawal periods and responsible medicine use.

Committed to antimicrobial stewardship, correct withdrawal periods and responsible veterinary medicine use.

Learn more about our company profile, browse veterinary pharmaceutical products or poultry health products, or read how learning shapes our quality standards.

Wide view of the Prix Pharmaceutica facility entrance and paved forecourt

Manufacturing

Built around controlled production.

Prix Pharmaceutica (Pvt) Ltd. works with manufacturing partners who meet our quality and regulatory requirements. All products are clearly labelled with their manufacturing classification.

Supported dosage forms

The current poultry catalogue lists powder, injectable, oral liquid and solution presentations. Other forms will appear here when they are added to the product data.

Manufactured for Prix Pharmaceutica (Pvt) Ltd.Marketed by Prix Pharmaceutica (Pvt) Ltd.Imported by Prix Pharmaceutica (Pvt) Ltd.Distributed by Prix Pharmaceutica (Pvt) Ltd.Partner manufactured

Prix Pharmaceutica (Pvt) Ltd. will only publish verified manufacturing capabilities. Contact us for specific manufacturing and sourcing information.

Facility

Manufacturing premises

Exterior views of the Prix Pharmaceutica manufacturing facility in Lahore, Pakistan. These photographs show the company premises and exterior manufacturing environment.

Main manufacturing building

Quality

Quality across the product lifecycle

Prix Pharmaceutica (Pvt) Ltd. applies quality controls throughout the product lifecycle, from raw material verification and production monitoring to finished-product testing, documentation and post-market surveillance.

  1. 01

    Raw material verification

    Raw material suppliers evaluated against quality and regulatory criteria.

  2. 02

    Production monitoring

    Systems and procedures that ensure products meet defined quality standards before release.

  3. 03

    Finished-product testing

    Laboratory testing of raw materials, in-process samples and finished products.

  4. 04

    Documentation

    Complete batch records supporting traceability and accountability.

  5. 05

    Post-market surveillance

    Continuous monitoring of product performance and safety post-distribution.

Batch journey and quality systems

The Prix Pharmaceutica (Pvt) Ltd. batch journey

  1. 01Material received
  2. 02Material quarantined
  3. 03Material tested
  4. 04Production approved
  5. 05In-process controls
  6. 06Finished product tested
  7. 07Documentation reviewed
  8. 08Batch released
  9. 09Product distributed
  10. 10Post-market monitoring

Quality systems

  • Quality Assurance

    Systems and procedures that ensure products meet defined quality standards before release.

  • Quality Control

    Laboratory testing of raw materials, in-process samples and finished products.

  • Batch Documentation

    Complete batch records supporting traceability and accountability.

  • Stability Assessment

    Products assessed for stability under defined storage conditions.

  • Supplier Qualification

    Raw material suppliers evaluated against quality and regulatory criteria.

  • Post-market Surveillance

    Continuous monitoring of product performance and safety post-distribution.

Certifications

Standards and documentation

Prix Pharmaceutica (Pvt) Ltd. will publish only verified and current certifications. Expired documents are shown as historical and are not presented as current certifications.

HISTORICAL / UPDATE REQUIRED

ISO 9001:2015

ACS Registrars Pakistan (Pvt.) Ltd. Certificate 193137

Expired 15 November 2025

This ISO 9001:2015 registration is not current. The catalogue certificate expired on 15 November 2025. An updated document is required before it can be presented as a current certification.

Request documentation
CURRENT

Certificate of Current Good Manufacturing Practices

Drug Regulatory Authority of Pakistan (DRAP). Ref. No. 179/2024-DRAP(AD-627190613556)

Valid through 08 May 2027. Pakistan-only.

Documented on the 2025 poultry product catalogue from a DRAP cGMP certificate issued 24 September 2024, following inspection on 08 May 2024. Validity is three years from the inspection date. The certificate is Pakistan-only. This page does not present an international GMP claim.

Request documentation
DOCUMENTED

Quality Management System

Internal QMS documentation and procedures

In place

Prix Pharmaceutica (Pvt) Ltd. maintains internal quality management system documentation and procedures. Contact us for specific certification information and documentation.

Request documentation

Certification information is currently being updated. Please contact Prix Pharmaceutica (Pvt) Ltd. directly for current registration and certification status. Product registration remains product-specific.

Regulatory

Regulatory framework

Prix Pharmaceutica (Pvt) Ltd. operates within the regulatory framework established for veterinary pharmaceutical products in Pakistan, including DRAP requirements for product registration, labelling and pharmacovigilance.

Product registration

Registration or approval is product-specific under applicable regulatory requirements.

Confirm the status of an individual SKU with Prix Pharmaceutica. This catalogue is not a blanket registration claim for every listed product.

Labelling compliance

Labels carry required information for veterinary pharmaceutical use.

Product labels contain all required information including active ingredients, dosage and withdrawal periods.

Pharmacovigilance

A system for collecting, reporting and evaluating adverse event reports.

Prix Pharmaceutica (Pvt) Ltd. maintains a system for collecting, reporting and evaluating adverse event reports.

Report an adverse event

Product complaints

A structured process for quality complaints.

A structured process for receiving, investigating and responding to product quality complaints.

Report a product complaint

Documentation

Complete documentation supporting regulatory compliance is maintained.

Complete documentation supporting regulatory compliance is maintained and available on request.

Import compliance

Imported products meet relevant veterinary pharmaceutical import requirements.

Imported products meet relevant import regulatory requirements for veterinary pharmaceuticals.

Responsible Use

Responsible Use

Responsible veterinary medicine use

Prix Pharmaceutica (Pvt) Ltd. is committed to the responsible use of veterinary medicines. We support antimicrobial stewardship, correct withdrawal period compliance and the responsible promotion and use of all products in our portfolio.

  1. 01

    Veterinary oversight

    All prescription products must be used under the guidance of a qualified veterinary professional.

  2. 02

    Approved dosage

    Always follow approved dosage instructions. Do not exceed recommended doses or treatment durations.

  3. 03

    Withdrawal periods

    Observe all withdrawal periods strictly before slaughter or before collecting eggs for human consumption.

  4. 04

    Antimicrobial stewardship

    Use antibiotics only when necessary, with appropriate diagnosis, and complete full prescribed courses.

Storage, records and reporting
  • Storage & handling

    Store and handle products according to label instructions to maintain efficacy and safety.

  • Record keeping

    Maintain records of all products used, dosages administered, withdrawal periods and treatment dates.

  • Product-label compliance

    Always read and follow the product label. Do not use products for non-approved indications.

  • Adverse event reporting

    Report any suspected adverse reactions or unexpected product effects to Prix Pharmaceutica (Pvt) Ltd. immediately.

Need technical product information?

Our team can help with product documentation, catalogue information and distributor enquiries.

Product and company inquiries

Need more information?

Speak with our team on WhatsApp for product, distributor and company inquiries.

+92 307 7867749