Medical writing plays a significant role throughout the lifecycle of pharmaceutical and healthcare products. It presents clinical and scientific data in not just a variety of formats, but also for various audiences. A regulatory writer’s work starts right from the product development process during its clinical trial phases and continues post release into the market through marketing and branding activities.
Taking your product from discovery to market is not easy and requires countless hours in paperwork and navigating the intricacies of regulatory compliance. Drafting documentation to adhere to the stringent guidelines is complex. Across every stage of your journey, 3Gen Consulting is here to help. With strong scientific expertise, skillful collaboration and efficient project management, our medical writers aim to empower your product and deliver quality documentation through our comprehensive medical writing services.
With a strong educational background and several years of experience, our medical writing experts are able to leverage their scientific expertise and creativity to develop customized content to engage multiple stakeholders and tell your product’s story.
From study protocols and investigator brochures to medical communication material, we provide a full suite of medical writing solutions with one goal in mind: Quality!
Our regulatory writers ensures that all documents are meticulously prepared to meet guidelines and remain compliant with standards set by regulatory bodies such as the ICH and FDA.
We understand the importance of clear communication and, wherever required, illustrated content in order to ensure that the complex information you are relaying is effective and high impact for your audience.
Clarity in documents and communication is critical to your success. As your partner, we understand that and set you up for success by managing your medical report writing challenges and providing quality deliverables that meet timelines and minimize costs.