White Paper - January 2025
The Vital Role of Literature Reviews in Pharmacovigilance
In today’s rapidly evolving pharmaceutical landscape, ensuring the safety and efficacy of medicinal products has never been more critical. Regulatory
requirements are increasingly stringent, and patient safety remains a top priority for stakeholders across the industry. Download our latest whitepaper to find out more.
White Paper - April 2024
Overcoming Barriers to European Market Access
In this whitepaper, we look at new solutions manufacturers are leveraging to scale the mountain of MDR clinical documentation requirements and the importance of leveraging new solutions to scale MDR clinical documentation for the EU market.
Tackling the MDR Transition
The Medical Device Regulation and In Vitro Medical Device Regulation, introduced by the European Union, have significantly reshaped the landscape of the medical device industry. Our latest white paper looks at how to tackle the MDR transition.
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