Additional services

Stability testing

Investigating the stability and shelf-life of a finished product is an important area of expertise at HeW Pharma Labo. We can assist you in defining the best approach for the study of the stability of your product, including accelerated testing, in-use or ongoing stability testing. Storage conditions in accordance with ICH guidance:

  • 5°C
  • 25°C / 60% RH
  • 30°C / 65% RH
  • 40°C / 75% RH

All testing is performed in our laboratory under the supervision of an independent study coordinator who manages your project. Moreover, if requested you will receive complete documentation of the stability. You can rely on our consultancy for regulatory support and assistance in the submission of applications. 

Chemical analysis

Our QC Laboratory is able to support your analytical needs from pharmacopoeial analysis of raw materials to finished products. HeW Pharma Labo can take over full analysis so that our customers can stay focused, even when they have limited internal capacity. HeW pharma Labo is equipped for the testing of a wide range of pharmaceutical forms (solid dosage forms, solutions, creams, oral sustained release forms, etc)

Cleaning validation

HeW Pharma is able to develop and validate analytical methods in the PPM range to support your cleaning validation. If needed, we can come on-site to assist you in taking swabs for cleaning validation. Both chemical and microbiological swabs can be taken to assist your cleaning validation activities.

Method development & validation

We develop scientifically sound and cost-effective analytical methods in co-operation with our customers. Services facilitating liable QC testing provided to our customers:

  • Development and implementation service for new products
  • Transfer of existing methods
  • Method Adaptation and Optimization
  • Method Validation