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July 01 2024
Upcoming RRD Webinar: Quality Systems Approach for Early-Stage Biopharma Companies

Don’t miss RRD’s upcoming webinar on July 18th, “Quality Systems Approach for Early-Stage Biopharma Companies,” presented by Nnamdi Nwachukwu. Learn best practices for getting to your first in-human trial, and ask your Quality questions at the Q&A.

July 18th at 1:00 pm ET. Register here.

The probability of success for a clinical trial can be greatly increased with proactive planning concerning the systems and logistics that will be used to house the clinical data. Proactive planning around systems and regulatory compliance can reduce risk and avoid unnecessary setbacks and missed milestones. Quality by design planning directly relates to the clinical and financial performance of clinical stage biotech companies.

Clinical Trials
Chemistry, Manufacturing & Controls
Information Systems & Validation
Document & Quality Management Systems
Knowledge Management & Training
Auditing & Compliance


Mr. Nwachukwu has 20 years’ experience spanning Quality, Computer Science, Regulatory, Manufacturing Engineering & Venture Capital. He has led over 50 GxP audits across 4 continents. Mr. Nwachukwu has led successful submissions for biologics, orphan drugs, vaccines and devices to FDA, EMA, TGA, ANVISA, MHLW & several Ministries of Health on the continents of Africa, Asia, Europe & South America.