Strategic & Business Services
Navigating Complex Markets and Unlocking Business Potential with Tailored Strategies for Growth and Innovation.
Navigating Complex Markets and Unlocking Business Potential with Tailored Strategies for Growth and Innovation.
We provide strategic and business services for the pharmaceutical and biotechnology industries, combining industry knowledge with strategic insights to deliver customized solutions for business growth and value creation.
Making strategic decisions and having business acumen are essential for success in the fast- paced biotechnology and pharmaceutical industries. The Strategic and Business Services offered by Zenovel offer professional direction and broad support in areas including due diligence, mergers and acquisitions, portfolio selection, in-and-out licencing, and client advising. Our services are intended to support you in achieving your strategic objectives, managing your portfolio optimally, and navigating challenging business environments.
We help clients to achieve their strategic and business goals, from portfolio optimization to profitable M&A transactions.
Team of advisors and consultants, with extensive industry experience, provides strategic insights based on industry realities.
We are dedicated to deliver highest quality of services.
We help you achieve your goals with our end-to- end strategic planning.
The European Union’s Good Manufacturing Practice (GMP) standards, as outlined in the Annex to the Guide to Good Manufacturing Practice for Medicinal Products, ensure the quality and safety of medicinal products, including those used in clinical trials. The Qualified Person (QP) plays a crucial role in batch certification, particularly for
In the intricate process of developing new pharmaceuticals, guaranteeing product safety, effectiveness, and adherence to global regulations is essential. Batch release testing acts as a pivotal quality assurance measure, confirming that medications comply with rigorous criteria before distribution. When combined with International Council for Harmonisation (ICH) standards, this testing framework
In the world of life sciences, quality isn’t just a benchmark—it’s the backbone of success. Three key pillars—Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Good Laboratory Practice (GLP)—form the core framework that supports everything from product development to regulatory approval. These standards aren’t just industry buzzwords; they’re the
In the pharmaceutical industry, quality is paramount—and at Zenovel, we are deeply committed to delivering excellence in Quality Assurance (QA). Our focus is on ensuring that every medicine is developed, manufactured, and delivered with safety and reliability as top priorities. QA is embedded in every stage of the pharmaceutical lifecycle—from
The U.S. Food and Drug Administration (FDA) emphasize the importance of data integrity in pharmaceutical manufacturing, particularly under its Current Good Manufacturing Practices (CGMP) rules. However, issues like fake lab results and sloppy record-keeping persist, posing risks to patients and losing confidence in the system. Independent oversight is crucial to
In the rapidly evolving pharmaceutical industry, assuring product quality and customer safety is a need. This endeavour continues to be based on validation, a methodical procedure to verify that manufacturing procedures and equipment consistently deliver high-quality outcomes. A strong strategy to validation is required in 2025 due to the complexity
