IDRE – Innovative Drugs Regulatory Europe GmbH

www.idremed.com

IDRE supports your product development IDRE is a global network of R&D professionals with years of experience in the development of pharmaceutical and biotechnology products. IDRE supports you in your early drug discovery The IDRE Team has long termed experience in the early stages of drug discovery. This ranges from identification and validation to selection and lead optimisation. IDRE identifies best KOLs for your drug development strategy KOLs are usually specialists in their clinical arena, and/or academic researchers prominent in their field. IDRE favoures the involvement of these specialists from the early stages of the development. IDRE selects the most pertinent CRO for your clinical trials Selecting a CRO for you to partner with is a critical decision; we use a process of evaluation that includes the below. The management of IDRE is aware that it is very difficult to change a CRO once the project has been initiated. IDRE manages your regulatory requirements We have our own regulatory experts (IDEA) around the world, as well as providing audit and inspection support (Rephine). In addition, they know and understand the nuances of regulatory affairs in their given countries, ensuring communications between sponsors and regulatory authorities are as seamless as possible

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Reach decision makers at IDRE – Innovative Drugs Regulatory Europe GmbH

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IDRE supports your product development IDRE is a global network of R&D professionals with years of experience in the development of pharmaceutical and biotechnology products. IDRE supports you in your early drug discovery The IDRE Team has long termed experience in the early stages of drug discovery. This ranges from identification and validation to selection and lead optimisation. IDRE identifies best KOLs for your drug development strategy KOLs are usually specialists in their clinical arena, and/or academic researchers prominent in their field. IDRE favoures the involvement of these specialists from the early stages of the development. IDRE selects the most pertinent CRO for your clinical trials Selecting a CRO for you to partner with is a critical decision; we use a process of evaluation that includes the below. The management of IDRE is aware that it is very difficult to change a CRO once the project has been initiated. IDRE manages your regulatory requirements We have our own regulatory experts (IDEA) around the world, as well as providing audit and inspection support (Rephine). In addition, they know and understand the nuances of regulatory affairs in their given countries, ensuring communications between sponsors and regulatory authorities are as seamless as possible

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Country

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City (Headquarters)

Munich

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Employees

11-50

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Founded

2020

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Social

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