Providing local competence and networks in all major pharmaceutical markets, our affiliates serve as points of contact for our customers as well as development and supply partners.
Midas Pharma GmbH
Midas Pharma France SAS
Our multidisciplinary team is committed to providing you with a wide variety of services.
We can provide you with your active ingredients, intermediates or drug products. We are here to help you with your projects and contribute to your success.
Indeed, Midas can support you in the following activities:
- Your development projects by providing you with:
- The reference products that are necessary for your bioequivalence studies and for your clinical studies, whatever the country of origin of the reference you need
- Active and intermediary principles for your developments
- All your current production activities by delivering the active ingredients and intermediates you need
- The creation and development of your drug portfolio by giving you access to dossiers and the supply of the finished products you are looking for.
In addition, Midas can also support you in your projects by offering:
- Development of your international business: through our various subsidiaries and our extensive network we can help you find the right partner that meets your needs.
- Development of your B2B out-licensing activity for finished products: we can promote your dossiers, in different regions of the world, using our different subsidiaries and our global Business Development team in order to quickly contribute to the development of your commercial activity.
- Co-development of differentiated and complex drugs: by taking advantage of the expertise that Midas has developed, particularly in drugs combining several active ingredients.
- Sale of assets (divestments): both for drug substance, drug products or for entire activities such as the withdrawal of a therapeutic class and for which you need an independent partner with the necessary contacts in order to objectively organize the best possible partnership and support you until the sales project is finalized.
We also offer other types of services depending on the regions in which we are present, such as: importing materials or medicines, managing logistics and storage, processing. This is why if you have a need, a question don’t hesitate to contact us so that we can together determine the service we can offer you.
Quality and reliability are key elements for us. By working with Midas, you benefit from our expertise, our subsidiaries and our international network of qualified partners with whom we have established long-term relationships. You can rely on us and delegate certain activities to us. By working with Midas, you can save time and resources to focus on what matters most to you. The purpose of Midas France is to support you and contribute to your business success and growth. We are available for you. You can contact us, or request an appointment.
Midas Pharma Italia S.r.l.
Midas Pharma Nordic
Midas Pharmaceuticals, Inc.
Midas Pharma Polska Sp. z o.o.
Midas Pharma Shanghai Representative Office
Midas can support you with the following activities:
- Access to key IM manufacturers in China
- > 100 reputable / reliable API & IM producers in our Chinese manufacturer portfolio, supported by our QM systems
- All suppliers covered by internal Principal Management, with a dedicated Sourcing Expert from Midas Shanghai, plus Reg Affairs- and QM Team Member
- Due to long-lasting relationships with Chinese manufacturers Midas has a profound knowledge about:
- Product portfolios
- Price strategies and cost situations
- Strengths and weaknesses in production, technologies and capacities
- Products under development, access to suitable starting materials and
- Reg Affairs / DMF status
- Inspection history (e.g. US-FDA, EMEA, PMDA, TGA, ANVISA)
- Previous customer audits
In addition, we can support you with our strengths in Quality Management:
As a result from all QM / Sourcing-Activities:
- Considerable amount of audit reports available
- Authority support already given or possible
- More than 1000 technical visits, mock audits, customer escort audits, inspection preparations, inspection escort audits, GAP analysis visits, CAPA follow-up meetings, on-site training sessions and commercial meetings already conducted.
Business Development Operations at Midas China
- Inlicensing of APIs – to China: à 13 active projects
- First own Midas-API in China approved
- Inlicensing of FDFs – to China: à 15 active projects
- Inlicensing Consumer Health Care products to China: à 6 active projects
- Outlicensing / Contract Manufacturing out of China: à 14 active projects
- EU MA Transfers, Authorized Generic Project Management, Own Developments for the Chinese Market and Brand Divestment Project Management
Quality and reliability are key elements for us. By working with Midas, you benefit from our expertise, our subsidiaries and our international network of qualified partners with whom we have established long-term relationships. You can rely on us and delegate certain activities to us. By working with Midas, you can save time and resources to focus on what matters most to you. The purpose of Midas China is to support you and contribute to your business success and growth. We are available for you. You can contact us or request an appointment.
Midas Pharma GmbH, Liaison Office India
Midas Pharma Liaison Office India can support you in particular with the following services:
- Sourcing of fine chemicals, key starting materials, intermediates and APIs from cGMP compaint Indian manufacturers.
- Supply of APIs, Intermediates, Key starting materials and fine Chemicals manufactured by our exclusive manufactuirng partners with complete regulatory documentation and GMP support.
- Supply of reference listed drugs (RLD) to Indian generic companies.
- GMP and GLP audits for gap analysis, pre-qualification audits, on-site and remote audits at manufacturers of key starting materials, intermediates, APIs and FDF (sterile and non-sterile) in India
We are also happy to support you with:
- Distribution and sourcing of key starting materials, intermediates, APIs and FDFs in and from India.
- Procurement of reference product (RLD) from various countries required for bioequivalence and clinical studies.
- Identification and project management with cGMP compliant Indian CROs and CMOs for the manufacture of fine chemicals, key starting materials, intermediates, APIs and FDFs (sterile and non-sterile)