Biosimilars 2018 - Overcome the current challenges, from development to pricing

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Regulatory Affairs and GMP compliance in Eastern Europe - Considerations for the EAEU and Non-EAEU markets

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Die Themen - EAEU pharmaceutical market: Regulatory Status quo - Registration of new drugs in the EAEU - Variations in the EAEU - CMC docum…

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Drug Market Access & Pricing in Europe - Payer Contracts, HTA process and Tender management

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Die Themen - Reference Pricing in Europe - Payer-Archetyping - Market Access and Pricing in France, Italy, Spain, Germany and the UK - Spec…

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EU Regulatory Affairs Introductory Training Course

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Die Themen - Day 1: Marketing Authorisation procedures in Europe: Legal basis, mutual recognition, decentralised and centralised procedure …

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Preclinical development: From bench to first in human - Regulations, data and study programs, transition to Phase I, small molecules and bi…

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Die Themen - Regulatory framework for the preclinical stage - Drug discovery and formulation development - Pharmacology, pharmacokinetics a…

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Blockchain for Healthcare Professionals [BTABKHP]

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OVERVIEW The Blockchain for Healthcare Professionals course reviews how Blockchain is being applied in the Healthcare industry. As the heal…

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e-Learning: Medical Device Advisor (MPDG) - according to § 83 MPDG: Training and e-Learning for non-German speaking employees

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Die Themen - European medical device law and its application in Germany - The MDR and IVDR - an overview of all relevant innovations for me…

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Biopharmaceuticals - Development, manufacturing and analytics of monoclonal antibodies and other proteins

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Die Themen Development & manufacturing on 24 June 2024: - Manufacturing process - Formulation - Process changes - Regulatotory requirements…

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Preparing for Mid-Term Review - Maximizing Impact and Planning Ahead

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Die Themen - Shifting allocations effectively within your programme - How to embed "Strategic Technologies for Europe Platform" (STEP) - In…

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Masterclass China: Medical Device Marketing Authorisation for Advanced - New regulations on medical devices, perfection of pre-market regis…

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Die Themen - Update your regulatory knowledge - Pre-Market Registration (PMR): Minimalise your efforts and costs - Acceptance of European r…

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Scaled Agile Framework 6.0: Leading SAFe (SA) - Classroom training

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Thrive in the digital age with Business Agility This two-day course gives you what you need to lead a Lean-Agile enterprise successfully in…