Providing services of stability testing, analytical testing, method development and validation, formulation development and QP release testing

Overview

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Our exciting new phase of development

Kemwell has entered into an exciting new phase of R&D Services. We are investing to expand the breadth and depth of our services to support projects from formulation to finished products. Our labs will be equipped for formulation and analytical development, including stability studies, method development and validation, etc. In Sweden, we can also provide services for QP release. Kemwell's sites in India and Sweden can work in harmony to provide you the best solution from both worlds.

Method Development/Validation
(Drug Substance, Drug Product, Excipients)

	Forced Degradation Studies
	Stability Indicating Methods
	Impurity and Degradation Product ID
	Preformulation Studies
	Method Transfers
QC Support
	EU Gateway Release and Testing: We offer this service to companies who wish to import products into the EU and require full analytical testing and QP release.

	Release Testing
	Stability Studies
	Reference Standard Qualification
	Cleaning Validation
	Microbial Testing
	Preservative Testing
Quality Assurance
Our experienced QA staff can provide quality assurance support and auditing for your internal or contracted studies. Our staff is experienced in auditing internal and external studies to assure compliance with GLP and/or GMP, as appropriate. They can also provide assistance in establishing new compliance programs.