New Member Spotlight: Dalfelt Clinical Trials Consultancy
We warmly welcome Ingegerd Dalfelt back, with her Dalfelt Clinical Trials Consultancy as a new member of our life science park, located in the co-working section of The Spark!
Dalfelt Clinical Trials Consultancy is the company experienced Ingegerd Dalfelt use as platform acting as a consultant, with 40+ years of experience turning complex science into compliant, high-quality trials. She's a proven leader across pharma and medtech, driving strategy, regulatory excellence, and execution – from concept to clinical evidence, supporting pharma, biotech, and academia. She also acts as full service CRO, for early-stage clinical trials.
We asked Ingegerd Dalfelt three key questions to highlight what makes her a trusted and versatile life science partner:
How can the life science community benefit from your membership at Medicon Village?
- With highest possible quality, audit readiness, and Sponsor oversight as main focus areas, I offer ICH and ISO 14155 compliant services and trainings, primarily to small and medium sized pharmaceutical and biotech companies, and academia to help them reach their goals.
- By combining flexibility with excellence, knowledge and long experience I am a dedicated and loyal partner to pharma/medtech companies and academia, driving company strategies through regulatory excellence and flawless execution to success.
Networking and Teamworking are the keys to success!
What makes Dalfelt Clinical Trials Consultancy stand out compared to competition?
- With 40+ years of experience in life science and a strong commitment to highest possible quality, innovation, and scientific excellence gives me a uniquely strong position to deliver guidance, advice, action and support.
- I am not only committed to deliver efficiently to my customers, but also offer long term, loyal partnership based on my long experience and competence.
- I can work as a full service CRO, either alone or together with my large network, within the fields of clinical development, medical writing, and regulatory affairs, with planning and management, to support in delivering success.
- I also offer support in developing and providing clinical Standard Operating Procedures and other useful regulatory compliant templates, mentoring, coaching, and on demand training courses.
- Patients always need to be a primary focus, so assisting in getting efficacious treatment, e.g., drugs and devices accessible to them gives great satisfaction and I am truly passionate about delivering results that matter for patients.
What are the current main challenges and opportunities in Life Science?
- The life science landscape continues to be a challenge, especially when it comes to financing and regulatory demands.
- This presents both a challenge and an opportunity for me to continuously evolve offerings to support partners navigating an expanding scientific and regulatory environment.
- By staying agile, science‑driven, curious, and customer‑focused, I remain dedicated to being the versatile partner that organizations can rely on, throughout drug and device development in an increasingly challenging, competitive and complex market.
For more information on how Ingegerd Dalfelt can support your next project, visit:
https://www.mediconvillage.se/member/dalfelt-clinical-trials-consultancy/