The Tapadar GmbH provides professional consulting and support in the area of Regulatory and Quality Affairs for pharmaceuticals, medical devices, food, dietary supplements and cosmetics. They support customers in mastering regulatory hurdles and can also act as a marketing authorization holder for pharmaceuticals.
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Industry:Management Consulting
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Consulting and operational support in Regulatory & Quality Affairs for medicines, food supplements and cosmetics; market access, regulations, laws and authorities.
Medicinal product authorisation and Life Cycle Management
Initial authorisation of medicinal products, Life Cycle Management and taking over the role of marketing authorisation holder in Switzerland.
Product development and marketability assessment for food supplements and cosmetics
Concepting new products as well as reviewing the marketability and labelling of existing products in the foodstuffs and consumer goods sector, in particular food supplements and cosmetics.
Taking over the FvP function (Switzerland)
Taking over the role of the technically responsible person (“fachtechnisch verantwortliche Person”) (FvP) in Switzerland for medicinal products and related regulatory responsibilities.
Project support for supplier and contract manufacturer qualification
Execution of projects such as the evaluation and qualification of suppliers and contract manufacturers in the pharmaceutical environment.
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