Case Study 01
Interim Head of Regulatory Affairs
Case Study 02
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03
The client did not have a dedicated regulatory affairs department, and they needed support in submitting a Marketing Authorisation Application (MAA). They sought consultancy support to set up a filing plan and lead a cross-functional team through the filing process.
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What the client asked for
Act as Interim Head of Regulatory Affairs
Support the upcoming MAA filing
Set up a filing plan & lead the cross-functional team through the filing
Build up the regulatory department
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How we supported the client
To support the client, we performed a gap analysis to identify critical resource gaps. We then closed some of these gaps by leveraging our network. We educated the team on filing requirements, processes, and potential critical steps. We developed a tailored filing plan, filing timetable, and key deliverables. We led the filing team meetings and managed ad-hoc issues on an ongoing basis.

Our support helped the client to successfully submit their MAA. We provided them with the guidance, expertise, and resources they needed to navigate the complex regulatory landscape and achieve their goals.

Strategic 
Regulatory
Advice
Interactions with Health Authorities
Submission
Management
Marketing
Authorisation
Application
Client quote
Stephanie @therainnova has been instrumental in guiding us through all aspects of the EU, US and MHRA filing process in her role as interim Head of Regulatory Affairs. She is a highly knowledgeable and experienced senior regulatory affairs leader with a dedication to meet the client`s deadlines and needs.
Dario Eklund
CEO, Santhera Pharmaceuticals
Client quote
therainnova has supported us in our EU MAA submission. Their swift and ad hoc support in preparing tabulated summaries for the EU MAA showcases their unwavering commitment to enable our timely MAA submission. We were very glad and thankful about their ad hoc support.
Omar Lahlou
Director Regulatory Affairs
Allecra Therapeutics
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Design by: G Design Studio
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© therainnova 2023