- Develop
and implement R&D and regulatory
strategy - Manufacturing and analytics strategy in compliance with cGMP requirements
-
Cost-effective
clinical development strategy
-
Support
to secure funding
-
Evaluation
of products, projects and companies in due diligences
Sobel Pharma Consulting understands
the constraints and hurdles that small pharma and biotech companies are faced
with. We are dedicated in providing
solutions to your product development and regulatory needs. Our goal is to help save resources and focus
on the results that generate maximum value for your stakeholders.
Sobel Pharma Consulting’s unique
“combined” scientific experience and knowledge enables us to manage all
processes involved in product development and regulatory approval. Furthermore, we are highly experienced in securing
funding from venture capitalists and private investors.
Sobel Pharma Consulting’s unique
features:
> More than 20 years of
experience in the pharma industry in the areas of production, clinical
development, regulatory and intellectual property.
> Expertise in a range of
products, including biosimilars, vaccines, cytokines, monoclonal antibodies and
fusion proteins. > Our consultants have
held senior positions in well-established biosimilar companies, such as
BioPartners.
> Highly personal and
cost-effective service
