Our medical affairs specialists bring unparalleled expertise and deep sector knowledge to champion your products every step of the way – from successful preparation for launch to effective life-cycle management. At tranScrip, we excel in empowering our clients through a comprehensive array of pre- and post-launch medical affairs initiatives spanning various therapeutic areas, including orphan diseases.
Throughout the lifecycle of your product, our robust medical affairs package ensures that your strategic planning and programme execution is not just comprehensive but transformative.
Maximise the value of your products with our bespoke solutions.
Our team excels in crafting comprehensive medical affairs strategies that align with your business objectives. We translate scientific data into actionable insights, creating purpose-built tactical plans that enhance market access and product lifecycle management.
We identify key stakeholders in the healthcare ecosystem, including clinicians, researchers, patient advocacy groups, and regulatory bodies. Our influence mapping techniques help prioritise engagement efforts, ensuring effective communication and collaboration with these critical partners.
We design and execute advisory boards, expert panels, and satellite symposia that foster meaningful dialogue between healthcare professionals. These forums provide valuable insights, validate strategic directions, and help shape the development and positioning of your products.
Our expertise extends to the meticulous planning and support for execution of late-stage clinical trials. We ensure that your studies are designed to meet regulatory requirements, generate robust data, and support your product’s value proposition.
We help you to create high-quality scientific communications, including manuscripts, review articles, abstracts, posters, and presentations. Our team works closely with you to develop compelling narratives that accurately convey your data and insights to the scientific community.
Transforming complex scientific data into clear, concise, and impactful messaging, we help you effectively communicate the significance of your research and products in a way that resonates with both medical professionals and broader audiences.
We offer tailored training programmes for your internal teams and external stakeholders. These sessions are designed to deepen understanding of scientific data, product details, and regulatory landscapes, ensuring that everyone is equipped with the knowledge they need to succeed.
Our teams collaborate closely with your global headquarters and local teams to craft and implement robust, compliant Medical Affairs strategies. We facilitate seamless interactions with external experts and opinion leaders, fostering productive cross-functional collaboration within your organisation.
Executive Director Medical Affairs, Regional Medical Lead, Hemato Oncology (Europe)
BeiGene
Our experienced physicians and scientists, together with our regulatory, clinical and commercial experts can support you to maximise the value of your products. Whatever your project requires, we have the expertise to meet your needs.