Manufacturing

We are committed to delivering quality products

Best Contract Manufacturing Pharmaceutical Company in India

Our Ultra-modern facility at SIDCUL, Haridwar complies with the WHO-cGMP & GMP standards and is spread over a 3600 sq. area. We have collaborated with the best API manufacturers and are equipped with the latest machinery to ensure timely deliveries and superior quality of products that have helped us to reinforce our position in the field of pharmaceuticals. We have got the best Air handling unit in the whole of Uttarakhand.

Our people are constantly being upgraded with the technical know-how and latest breakthroughs in the pharma industry so as to implement high – quality systems across our manufacturing facilities thus ensuring consistent quality and efficacy of our products.

Our Infrastructure

Our Capabilities

  • The Ultra-modern facility as per GMP standards spread over 3600 sq. area.
  • World-class machinery with high production plant capacity per shift per annum:
  • a. Tablet Section: 374.50 million Tablets
  • b. Capsule Section: 46.80 million Capsules
  • c. Liquid Section: 15.60 million Bottles
  • d. Sachet Section: 3.12 million Sachet
  • e. Dry Powder Suspension: 4.68 million Bottles
  • f. Tubes Section: 5.0 million Tubes
  • g. Lotion Section: 1.0 million Bottles
  • In–house product testing

Dosing Forms

Quality:

Rivpra is committed to delivering affordable and high-quality products and it is embedded at every stage of our operations. We aim to meet and exceed the expectations of our stakeholders, marketing companies, government institutes, and export parties by implementing a robust quality management system by conforming to cGMP standards.
We have deployed the best technical team in QC, QA, and production departments to carry out the Manufacturing Operations Analysis. The total quality Management System is designed to ensure ‘No Defect Product’.

We have a fully equipped in-house testing facility to control and keep a regular check to ensure the best quality. Our quality practices include:

1. Quality system management:

• Testing of raw and packaging materials as per SOP.
• Testing of in-process samples
• Testing of finished goods
• Carrying out stability studies

2. Regular quality audits to identify and eliminate defects

3. Quality risk control