Showing 13666 to 13680 of 22847 results
12th Edition Market Driven Innovation

12th Edition Market Driven Innovation

07 - 09 November, 2022

Berlin, Germany

Capitalize on market opportunities through building an innovation strategy that includes collaboration, disruptive technologies and the latest consumer insights. The marcus evans 12th Edition Market Driven Innovation conference taking place on 7-9 November, 2022 in Berlin, Germany, will showcase real life case studies of how companies have transformed their innovation process to align with key market drivers, enhancing the overall resilience, ...

  • +4 months

Senior Formulation/Product Manager - Futures

Nomad Foods

Senior Formulation/Product Manager - Futures in Lowestoft, Suffolk | Careers at Lowestoft (icims.com) This role is known for lead the Futures R&D Product and Formulation workstream t...

Lowestoft, Suffolk, UK

  • +6 months
Patient Engagement in HTA Processes MasterClass

Patient Engagement in HTA Processes MasterClass

15 - 16 September, 2022

Online Event

The purpose of this Master Class is to sensitize participants for the value patient engagement and provide a brief introduction on the practicalities of patient engagement in HTA processes. 15 - 16 September, 2022, Virtual Time Zone: UTC/GMT+1 /CET Key Elements: Understand the current and potential future impact of including patients’ perspectives. Understand current state of patient engagement in HTA processes in vario...

  • +6 months
Pharmacovigilance Audit and Inspections US MasterClass

Pharmacovigilance Audit and Inspections US MasterClass

13 - 15 September, 2022

Online Event

The training will explore the key aspects of pharmacovigilance audits (PV Audits), from planning audit programmes, conducting audits to delivering audit findings through audit reports. The impact of the pv legislation and GVP will be addressed and guidance will be provided. Key Elements: Understand different types of audits. Assessment criteria for auditing. Key principles on audit design and preparation. ...

  • +6 months
Behavioral Good Manufacturing Practices MasterClass

Behavioral Good Manufacturing Practices MasterClass

19 - 20 September, 2022

Online Event

The main goals of this online masterlass are based around improvements in GMP compliance and error reduction. Key elements: Understand the need for cultural change when managing our GMP compliance. Measure the Cost of Compliance in our manufacturing operation. Overview of the bGMP cultural change programme. Understand the different models of human error, human thinking processes and actions. ...

  • +6 months
Clinical Project Management MasterClass

Clinical Project Management MasterClass

26 - 29 September, 2022

Online Event

During these 4 day online masterclass, Trainees will learn how to adapt their project management knowledge to clinical trials.  Key Elements: What are the fundamentals of Project Management? The Project Manager (negotiation, delegation, dealing with clients, quality)? The Project Environment (regulations, guidelines, SOPs) The clinical development Plan. The definition and initiation of a Trial (scope, feasibility, CDP) How...

  • +6 months
Viral Clearance MasterClass

Viral Clearance MasterClass

03 - 04 October, 2022

Online Event

This online masterclass will give an overview of the sources and impacts of viral contaminations of biotherapeutics, how to prevent those risks and how to evaluate the capability of the process to remove and/or inactivate potential viruses through viral clearance studies.  Key Elements: Understand the consequences linked to a contamination of mammalian cell cultures and biologicals Understand the regulatory expectations on prev...

  • +6 months
Advanced CMC MasterClass

Advanced CMC MasterClass

05 - 06 October, 2022

Online Event

This training will present Technical and regulatory requirements for developing a medicinal product which are becoming stricter every day, the products themselves become more and more complex.  Key Elements: Understand the different levels of requirements in CMC during the development and post-approval phase. Overview of stability requirements. Understand what are the Essential Requirements for a Drug Substance. ...

  • +6 months