Kapynag Pharma Pvt Ltd

Manufacturing Facility

Designed as per the WHO-GMP requirements

Constructed in eco-friendly environment over 7000 sq. meter area

Modern quality control department equipped with HPLC, UV etc

Dedicated microbiology, analytical laboratory, R&D and F&D setup

Well established HVAC, RO Water and Compressed Air Systems

Research and Development

In-house Research and Development facility is equipped with latest technologies together with trained and experienced team

Our qualified workforce with well-equipped laboratory nurtures every single project from initial stage of development till commercial production

Quality Assurance and Quality Control

Well defined Quality Management System

Equipped with latest technology and advanced instruments enabling all Pharmacopoeial testing in-house

Trained and experienced quality management professionals

Rigorous testing regimens across all production stages, all put together ensure quality healthcare products at every stage of production

Our quality systems, policies and procedures are designed to ensure consistent product quality and compliance

Regulatory Affairs

At Kapynag, we have a dedicated and qualified team to support regulatory affairs

Providing a complete range of regulatory documents suitable to the client's requirement

Preparing and filing dossiers in consultation with the client's regulatory group for semi-regulated and advanced markets

Tracing the submission with different regulatory bodies and client's regulatory group

Liaison with state FDA and other governing bodies for getting necessary product

permission and other quality related certificates and approvals

Manufacturing Capabilities

Adverse Event Reporting

Kapynag is strongly committed to manufacturing and providing quality products. However all medicines have their benefits and associated risks. We would like to hear from you in case of any adverse reactions from products manufactured by Kapynag. This will help in continuous monitoring of product safety.

What is an Adverse Event?

Adverse Event is defined as an undesirable medical condition that can be symptoms, signs or any abnormal results of an investigation. Adverse Events are not necessarily caused by the medication – the event needs to have occurred after taking a medication in question.

What to report?

Any adverse drug reaction/side effects noticed or diagnosed after consumption / application of products manufactured by Kapynag Pharma.

Where to report?

To report adverse drug reaction contact our customer care: info@kapynag.com

Leading WHO-GMP certified Pharmaceutical Company Specialising in Third Party/Contract Manufacturing

Manufacturing Facility

Research and Development

Quality Assurance and Quality Control

Regulatory Affairs

Manufacturing Capabilities

Adverse Event Reporting

What is an Adverse Event?

What to report?

Where to report?

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