Provides Consultation in Development, Manufacture & Regulation of Biological Products in a Dynamic 21st Century Risk-based Regulatory Environment with focus on Total & Sustainable Quality & Compliance based on Science & Law for the International Market, using Concepts of Quality by Design (QbD) & Risk Management Approaches to exceed Minimum Requirements. Combining Scientific & Regulatory Expertise with Strong Mentoring, Motivating & Decision-making Skills, and Using Modern Technologies, Strategic Planning result into achieving Vision & Mission of the Organization
BQRC Difference & Strengths
Vaccines
Vaccines are Unique and Complex Drugs because these are given to Healthy Population. Development and Manufacture of Vaccines of Consistent Quality require in-depth Knowledge and Understanding of Science, Regulations and Principles of Quality & Biological Standardization.
Blood-Derived Products
Blood-derived Products are Historical Biologics, going back to more than a century, Starting with Products made in Horses and shifting to Human Blood-Derived Products. Ensuring Quality of these products from the Starting Material is Critical in Safety of these Products.
Therapeutic Proteins
Genetic Engineering and Recombinant Biotechnology revolutionized generation of Therapeutic Biologics, reducing Human sufferings and Disease Burden. These products brought analytical technologies and new innovations to the manufacture of biologics.
Monoclonal Antibodies
Discovery of Monoclonal Antibodies in 1975 have brought treatment to many diseases that seemed incurable or did not have effective treatments. Monoclonal Antibodies and therapeutic proteins brought the Concept of Well-Characterized Biologicals.
Biosimilars
Biosimilars bring affordable Therapeutic Proteins and Monoclonal Antibodies to patients. Vaccines and Blood-derived Products have been historical biosimilars. Success of Biosimilars depends upon sound biological standardization and analytical comparability.
Cellular Tissue & Gene Therapy Products
Cellular, Tissue and Gene-Therapy Products are the Cutting-Edge and Most Innovative Biologics that require creative and out-of-box characterization tools based on sound science.
Total Sustainable Quality and Compliance
Strategic Planning Development & Licensing
Analytical & Serological Methods
Implementing Modern Technology in Testing
Strong Understanding of science & Compliance
Theoretical Knowledge & Practical Experience
Class-Room & Hands-on (On-Site) Training
Mission
Our mission is to use our expertise to advance the development, manufacture, and regulation of biological products, especially vaccines. We aim to accelerate the delivery of safe, innovative biological products to the public to prevent and reduce disease impact. By combining cutting-edge science with strict regulatory standards, we expedite product availability and enhance quality of life through better health outcomes.
Vision
BQRC aims to be a key player in ensuring global quality and compliance in biological product manufacturing. We help clients meet international regulatory requirements for safe, impactful biological products. Our vision includes collaborating with academic institutions, non-profits, and international organizations to support vaccine development, particularly in resource-limited settings, often providing pro bono services.
Philosophy
We navigate the complex global regulatory environment for biological products by adhering to local and international guidelines, including those from the World Health Organization. Our approach focuses on strategic planning to streamline regulatory processes, reduce redundancy, and facilitate market entry. We are committed to maintaining high quality standards throughout the product lifecycle, from development to licensing.
Welcome to Biologics Quality & Regulatory Consultants, LLC (BQRC), a leading business consulting firm based in North Potomac, MD. Specializing in the quality, regulatory, and compliance aspects of biologics, BQRC is your trusted partner in navigating the complexities of biologics development, manufacturing, and ...
Achieving total quality and sustainable compliance for biologics in a dynamic regulatory environment, including current Good Manufacturing Practices (cGMP), requires not only expertise in relevant regulations and laws but also a deep knowledge and practical experience in the development and manufacture of these ...
Use the contact form below to submit your inquiry, and our consultants will respond with tailored advice and solutions to help you manage and excel in your biological product endeavors.
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