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Type: Think Tanks

Think-TankTrabsparency-landscape-January-2019-NC-1
Navigating the Global Transparency Landscape
January 24, 2019 | North Carolina, US Trilogy hosted a discussion on the implications that the disclosure and transparency regulations will have on producing clinical regulatory documentation and provided insight...
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Taming the Complexity of Preparing CTD Submission Dossiers: Science meets Logistics
October 25, 2019 | Massachusetts, US Trilogy hosted a discussion on how to make the process of writing and coordinating a CTD submission dossier as efficient as possible and, ultimately,...
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Writing Lay Summaries
January 22, 2020 | London, UK Trilogy hosted a discussion on writing Lay Summaries and their experience on how to overcome the unique challenges found when writing these types of...
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Writing Lay Summaries
November 05, 2020 | Virtual Trilogy hosted a discussion on writing Lay Summaries and their experience on how to overcome the unique challenges found when writing these types of documents.
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Taming the Complexity of Preparing CTD Submission Dossiers: Science Meets Logistics
Trilogy hosted its second virtual Think Tank on how to make the process of writing and coordinating a CTD submission dossier as efficient as possible and, ultimately, reduce the stress often associated with this activity.
Think-Tank-Dossiers-London-2019 (1)
Taming the Complexity of Preparing CTD Submission Documents: Science Meets Logistics
April 26, 2019 | London, UK Trilogy hosted a discussion on how to make the process of writing and coordinating a CTD submission dossier as efficient as possible and, ultimately,...
Transparency-requirements-for-clinical-documents-london-2018
Transparency Requirements for Clinical Documents
September 21, 2018 | London, UK Trilogy hosted a discussion on the implications that the disclosure and transparency regulations will have on producing clinical regulatory documentation, together with our speakers:
Responses-to-Regulatory-Authorities-think-tank-NC-March-2018
Responses to Regulatory Authorities: Measure Twice - Cut Once
March 15, 2018 | North Carolina, US Trilogy hosted a discussion on how to make the process of writing and coordinating these responses as efficient as possible, together with our...
the-clinical-development-plan-think-tank-Frankfurt-December-2017
The Clinical Development Plan - A Map to Faster and More Successful Approval
December 14, 2017 | Frankfurt, Germany Trilogy hosted a discussion on the main advantages of the CDP, as well as the main challenges on writing this document and possible solutions,...
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PBRERs and RMPs
November 14, 2017 | London, UK Trilogy hosted a discussion on the main challenges on PBRERs and RMPs and reviewer insights, together with our speakers:
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Measuring the Service of Medical Writing
October 31, 2017 | North Carolina, US Trilogy hosted a discussion on the challenge of measuring the service provided for medical writing – how do you define a good quality...
Measuring-the-Quality-of-medical-writing-think-tank-london-november-2016
Measuring the Quality of Medical Writing
November 29, 2016 | London, UK Trilogy hosted a discussion on the challenge of measuring the service provided for medical writing – how do you define a good quality document...
Risk-management-plans-and-summary-for-the-lay-reader-think-tank-Frankfurt-July-2016
Risk Management Plans and Summary for the Lay Reader
July 12, 2016 | Frankfurt, Germany Trilogy hosted a discussion on every-day challenges involved in meeting the guideline on good pharmacovigilance practices (GVP), the challenge of writing and managing Risk...
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The Patient's Voice Through Social Media
December 15, 2015 | London, UK Trilogy hosted a discussion on “Are we ready for the patient’s voice through social media in the benefit-risk assessment of drugs?” amongst a small...
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Measuring the Quality of Medical Writing
November 3, 2015 | Frankfurt, Germany Trilogy hosted a discussion on the challenge of measuring the service provided for medical writing – how do you define a good quality document...
Good-Pharmacovigilance-Practices-Think-Tank-London-June-2015
Good Pharmacovigilance Practices
June 18, 2015 | London, UK Trilogy hosted a discussion on the challenges posed by the guideline on good pharmacovigilance practices (GVP) with a special focus on Risk Management Plans...
Market-Access-and-reimbursement-think-tank-Frankfurt-2015
Market Access and Reimbursement
April 23, 2015 | Frankfurt, Germany Trilogy hosted a discussion during which we explored strategies for how to make sure that your Clinical Development Programme meets not only the needs...