@dokumeds

@dokumeds has been a member of Linktree for 4 years and joined in July 2021. The social media accounts linked to from @dokumeds are: Facebook, Instagram, LinkedIn, Email, X. Besides social media accounts, dokumeds has populated their site with Dokumeds.com, 6 Tips for Managing Clinical Trial Logistics in Russia, 5 Key Considerations for Planning Paediatric Clinical Trials in the EU, GDPR and Clinical Trials: Data Transfers within EEA (European Economic Area) and to Third Countries, How to Minimise Change Orders, Clinical Trials in Oncology - Key Points to Consider, Adapting to Cultural Differences to Positively Impact Clinical Trials, Pros and Cons to Working with a Mid-Size CRO, Increasing Clinical Trial Enrollment Through Innovative Digital Techniques, Tackling Risks Related to Unforeseen Project Costs, Medical Devices: Are You Ready For EU MDR 2017/745?, Emerging Increase in Medical Science Liaisons in Clinical Development, Clinical Trials in Ophthalmology, Scientific and Medical Expertise for Successful Clinical Development, COVID-19 Implications on Clinical Trial Site Auditing, Overcoming Challenges in Rare Disease Clinical Research, CRO Project Manager Retention as a Key Factor for Clinical Trial Success, E-BOOK: The Ultimate Guide to Pharmacovigilance in the EU, COVID-19 Impact – Enrollment in Clinical Trials, E-BOOK: Oncology Clinical Trials in Europe: Complete Guide, Employee Training Programs as a Quality Improvement Tool for Clinical Trials, Overcoming Risks to Clinical Trials during Pandemics, A Short Summary of the Regulations for Clinical Trials Across the EU – Upcoming Changes & Considerations, Defining the Request for Proposal (RFPs) Process for Clinical Trials, How to keep Clinical Trials on Budget, Outsourcing Tuberculosis Clinical Trials, Ensuring On-time Patient Recruitment in Clinical Trials, 5 Ways Dokumeds Improved Study Start-up Times in Russia, The Importance of Finding New Vaccines and Drugs to Fight Tuberculosis, Dokumeds Passes GDP and ISO Surveillance Audits, E-BOOK: Paediatric Clinical Trials in the EU: How to Overcome Regulatory and Ethical Challenges, E-BOOK: Understanding the Supply Chain and Customs Regulations in Russia, The Importance of Scientific Advice from the Regulatory Authorities in Clinical Research, E-BOOK: A Roadmap to Navigate Regulations for Clinical Trials in the European Union, How to Successfully Outsource your Pharmacovigilance, WEBINAR: Accelerate your Trials with Efficient Enrolment, Dokumeds’ Expansion into South Africa, Dokumeds opens an office in South Africa, Discover Russia with Dokumeds: Regulatory Submission Overview in Clinical Trials, The Importance of CTA’s in the Clinical Research Process.