Supporting you and your projects
Our services
Medaptive can help you with every step of the medical review process, from helping to plan the development of your projects, through to aftercare and ongoing support for your brands.
Planning your project
We help support you with medical review and approval activities related to products in development.
We are here to assist your medical and commercial teams navigate through compliance complexity for products in early phase development. This ensures activities such as advisory board meetings, and presence and further requirements at congress and conferences during this time are carried out in a compliant manner.
Launching your project
Medaptive has extensive experience in working with marketing teams to develop both promotional and non- promotional assets for your company’s products. Our knowledge can help you develop healthcare professional and patient focused materials including patient support programmes for a product launch.
Additionally we offer assistance with product launch meeting activities, attendance at speaker briefings and moderation of questions from participants at live or virtual events.
Beyond launch and aftercare
Do you have a new campaign for a product or a disease awareness activity you are looking to roll out, or a prescribing information update that requires multiple materials for review?
We can provide you with resource to help during times of limited medical review and signatory capacity or as ongoing support for your brands.
Would you like to save time with our expertise?
We’d love to hear from you.
Contact us
Our experience compliments our services
Our breadth of experience caters from small biotech companies focused on rare diseases through to large pharmaceutical enterprises in highly competitive environments.
Our team has extensive experience in supporting our clients with one-off campaign/task support, to building sustainable relationships from pipeline to post-launch on project activities. Medaptive’s core foundation strives to create an integrated, high quality and reliable partnership with you.
We aim to compliment your company by taking the time to invest in our medical review team members. We ensure a current, dedicated, valued service that’s best fitting to your needs, ethos and environment.
Our extensive knowledge of the ABPI, IPHA, EFPIA and IFPMA Codes of Practice makes us the ideal partner for projects at a global level as well as local UK review initiatives.
Understanding you and your ideals
Whether a one-off activity or a client looking to build a sustainable relationship on current and future projects, Medaptive’s core ethos lays a solid foundation for a reliable and high-quality partnership.
We will invest our time with you
We ensure dedicated medical support that best fits the project, ethos and the environment to complement your company and add value to the service we provide.
We don’t use set packages
Our bespoke support empowers you to make informed decisions confidently at the right time.
It is our symbiotic approach that has earned Medaptive the reputation where much of our business comes from returning clients and recommendations.
Contact us with your review and approval requirements (or) medical affairs requirement to see how Medaptive can help you.
From fact finding and recognising requirements during initial meetings, to post launch support where the communication is still ongoing; we make the time to nurture client relationships to promote growth and development.
You will be working with a member of the Medaptive team who will become an expert in your product/project making the process of not only the project at hand, but future collaborations cost effective and efficient.
We appreciate and respect your business. Our collaboration is more than the delivery of projects. We ensure our success by adapting to work as a team within your organisation. There are no set packages.