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HWI group

The HWI group is an innovative and independent partner of the pharma and biotech industries. Today we offer our services for active ingredients, medicinal products and associated products at our sites in Rülzheim, Frankfurt and Appenweier.

HWI group

The HWI group provides a wide range of individual and specialised pharmaceutical services for the pharma and biotech industries, in particular for active ingredients and medicinal products.

Quality management

Quality management is a critical and strategic factor for us. We meet all the requirements stipulated in quality-control and quality-assurance regulations. Find out here what we do to achieve the highest possible quality and how we live by these requirements.

Contacts

You can find an overview of our contacts in different divisions here. However you can also simply ask our main office and we will connect you with the right person.

Media centre

Videos and live streams of HWI group are available in our media centre. Discover movies providing insights into the company and our services.

News

Companies that grow and develop have people who work towards this on a daily basis. A lot happens at the point where people and work mix – and that’s what we want to report. The most important news can be found here.

Funding

HWI group projects supported by funding programs.
Services
- Laboratory
  
  Laboratory services
  
  Development and validation
  
  Analytics of Biologics
  
  Impurities
  
  Stability testing
  
  Reference standards
  
  Product range reference standards
  
  Laboratory
  
  We are your partner for pharmaceutical analysis and quality control. Our 30 years of experience mean we offer the highest quality analytical services for active ingredients, excipients, medicinal products and drug-related products in our GMP- and FDA-certified laboratories.
  
  Laboratory services
  
  We are your partner for pharmaceutical analysis and quality control. Our 30 years of experience mean we offer the highest quality analytical services for active ingredients, excipients, medicinal products and drug-related products in our GMP- and FDA-certified laboratories.
  
  Development and validation
  
  We develop and validate test methods for identity testing, assay, purity testing and in vitro dissolution for active ingredients, excipients, intermediates, ready-to-use products and medical devices in accordance with international regulatory requirements and the latest scientific and technical knowledge.
  
  Impurities
  
  In addition to method development and validation to determine synthesis by-products and degradation products, we are specialised in the field of impurity trace analysis.
  
  Quality control
  
  In our GMP- and FDA-certified laboratory we conduct analytical testing as part of batch release for active ingredients, medicinal products and drug-related medical devices. We can undertake all your stability testing: storage, analytical testing and stability report as part of ICH studies and follow-up studies.
  
  Reference standards
  
  We have been involved in the preparation, purification and qualification of pharmaceutical reference standards for 30 years. This knowledge and experience makes us the ideal partner for your reference standards needs.
  
  Product range
  
  Our reference standard product range covers a wide range of qualified primary and working standards at a cost-effective price–performance ratio.
- Drug development
  
  Drug development
  
  Small batches
  
  Clinical trial batches
  
  Product life-cycle
  
  360°Cleanroom
  
  Drug development
  
  In formulation development, we offer galenic and analytical development for solid, semi-solid and liquid dosage forms.
  
  Drug development
  
  In formulation development, we offer galenic and analytical development for solid, semi-solid and liquid dosage forms.
  
  Small batches
  
  In the manufacturing area, we specialise in the production small market batches under GMP conditions.
  
  Clinical trial products
  
  In the manufacturing area, we specialise in the production of clinical trial products under GMP conditions.
  
  Product life-cycle
  
  Market changes and constantly changing regulatory requirements place manufacturers under permanent pressure to adapt or optimise medicinal products that are already being marketed. We provide you with support to successfully implement change management.
  
  360°Clearoom
  
  Take a look at our heart of drug development. State of the art technological equipment enables the processing of high potent active ingredients.
- QP services
  
  QP services (GxP)
  
  Regulatory services
  
  QP services
  
  Our interdisciplinary team offers all services relating to QP services, quality management and batch release.
  
  QP services
  
  Our interdisciplinary team offers all services relating to QP services, quality management and batch release.
  
  QP services
  
  We provide advice on how to meet quality management requirements in accordance with legislation and hold our own manufacturing authorisation for the release of market and clinical batches of medicinal products.
- Pharmacovigilance
  
  PV services
  
  Pharmacovigilance
  
  Based on good pharmacovigilance practice (GVP) recommendations we provide comprehensive and individual support for all pharmacovigilance matters.
Services

The HWI group provides a wide range of individual and specialised pharmaceutical services for the pharma & biotech industries, in particular for active ingredients and medicinal products.
Careers
Blog

News

News

Stay up-to-date. In our news section we regularly inform you about the latest news from HWI group.

21. December 2021

Merry Christmas

The second year in a row was challenging for all of us in many ways. As the year comes to an end, we are pleased to be able to look back on a good and satisfactory year.

Read more … Merry Christmas

25. November 2021

We are proud to present our new SEM-EDX system

SEM-EDX combines high-resolution imaging with elemental identification in a spatial manner.

Read more … We are proud to present our new SEM-EDX system

28. September 2021

HWI blog: The way of process digitalisation in pharmacovigilance

HWI group is being completely digitalised ICSR processing in pharmacovigilance. What are the main advantages of a digital process flow and how does low-code / no-code help to digitalise complex processes in an interdisciplinary setting? Get all the answers in our HWI-blog by Dr Lisa Held and Thomas Wessling

Read more … HWI blog: The way of process digitalisation in pharmacovigilance

14. June 2021

Coronavirus measures of the HWI group

Until further notice, the HWI group will take the following measures to ensure that our services are maintained for you.

Click on "Read more" and read the measures in detail.

Read more … Coronavirus measures of the HWI group

11. May 2021

#Mediathek

Video -> Drug Development

Have a look: In our video you get an overview of our services in drug development

Read more … Video -> Drug Development

19. April 2021

HWI blog: Troubleshooting

Unexpected quality problems in pharmaceutical manufacturing require a reliable root cause analysis as well as quality and safety assessment followed by the definition of preventive measures to avoid such incidents.

Find out what this means in detail in our HWI-blog by Dr Sandra Huertgen.

Read more … HWI blog: Troubleshooting

08. January 2021

30 years HWI

30 years ago: On January 8^th, 1991, the company was founded by Dr. Stefan Wissel and Prof. Dr. Hanns Häberlein. The two university friends created the name HWI from the first letters of their last names.

Read more … 30 years HWI

21. December 2020

#PressRelease

Expansion of the Management Team

As of January 1^st, 2021, Dr Frank Böttcher will be appointed to the management team of HWI pharma services GmbH and will strengthen the current management team of Dr Stefan Wissel and Dr Melanie Kerst.

You will find further information in our press release.

Read more … Expansion of the Management Team

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How to find us

Appenweier site

Contact

+49 7272 7767-0

info@hwi-group.de

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Hotline

Monday - Friday

+49 7272 7767-0