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GMP is in our DNA – we take your products from idea to market success.

We build bridges – from idea to market success

<strong>Development</strong><br /> Refined to top quality
Our core competency is refining raw materials for your needs and finding extraction methods for plant-based starting materials.
Development
Refined to top quality
<strong>Sourcing</strong><br /> reliable and exclusive
Hänseler Swiss Pharma has access to exclusive trade sources and a longstanding supplier network.
Sourcing
reliable and exclusive
<strong>Manufacturing</strong><br />as individual as you are
We offer a wide range of options for liquid, semi-solid and solid products using modern, flexible manufacturing. We are also experts in processing hazardous substances.
Manufacturing
as individual as you are
<strong>Packaging</strong><br/>flexible and in any size
We offer GMP-compliant packaging in a wide range of primary and secondary containers, as well as industrial containers – all perfectly aligned with your needs.
Packaging
flexible and in any size
<strong>Market access </strong><br/>250'000 customer contacts a day waiting for you
We assist you with authorisation, clarification of product status and all distribution- and market-side activities in the Swiss healthcare market.
Market access
250'000 customer contacts a day waiting for you

Discover our core competences

Individual drops fall into still water as a symbolic image for Hänseler Swiss Pharma Liquid Solutions
Detailed photo of an ointment as a symbolic image for Hänseler Swiss Pharma Semi-Solid Solutions
Detailed photo of a white powder as a symbolic image for Hänseler Swiss Pharma Solid Solutions

Our expertise, your success

Regulatory and customer requirements are increasing the significance of documentation. We regard documentation both as a quality certificate for our products and as a service to our customers. We therefore provide a range of documentation packages.

Documentation packages for active pharmaceutical ingredients

ASMF Package (Active Substance Master File)
CTD Module 3 – Part 3.2 S 
Technical Package
Documentation for CTD Module 3 – Part 3.2 S:
 
  • General information such as nomenclature and structure
  • Flow chart preparation 
  • Stability data
  • Sterility testing
  • Documentation for starting substances (SDS, other technical documents)
Phyto Package
Statement for CTD Module 3 – Part 3.2 S:
 
  • Analytical certificate with full supply chain
  • Harvest protocol
  • Certificate of origin
  • Documentation for starting substances (SDS, other technical documents) 
  • Testing for pesticides, heavy metals and aflatoxins 
  • Pyrrolizidine alkaloids 
  • Microbiology
  • Flow chart preparation 
  • Stability testing to customer specifications

Documentation packages for finished pharmaceuticals

Documentation packages for finished pharmaceuticals
CTD Module 3 – Part 3.2 P 
Compiling the necessary documentation in accordance with customer instructions.

Documentation packages for cosmetic products

Documentation packages for cosmetic products
The package contains all the documents needed to create a PIF. On request, we can also commission safety reports.

Documentation package for excipients

Documentation package for excipients
The package covers excipient requirements to ICH Q9.