RLM Consulting

What we do: RLM Consulting specializes in providing strategic and operational regulatory affairs support to bio-pharmaceutical companies developing medicinal products. Their expertise covers the entire product development lifecycle, from early nonclinical research through preclinical and clinical testing, to registration, launch, and post-marketing activities such as pharmacovigilance and variations. They focus on helping small and medium-sized biotech firms navigate complex regulatory landscapes in the EU and US, offering tailored guidance for regulatory approval and negotiations with authorities like the EMA and FDA.

Where we are located: The company is headquartered at Rue Louis de Geer 6, 1348 Ottignies-Louvain-la-Neuve, Belgium.

Short history: Founded in 2006, RLM Consulting has built a solid reputation in regulatory affairs and drug development. Over the years, it has grown into a specialized consultancy known for its expertise in regulatory strategy and negotiation with national agencies and international authorities.

Organization & culture: RLM Consulting employs around 21 experts, including highly skilled scientists with backgrounds in biology, chemistry, pharmacy, clinical research, and business. The company values integrity, collaboration, and excellence, fostering a culture of open communication and professional growth. Their team is passionate about advancing science and improving patient lives through innovative medical products.