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Examples of the Many EAS Authored Articles Found on our Website
- EASeNews: Big Data, Real World Evidence and The Digital Revolution – Hang On!
- EASeNews: Good Manufacturing Practices – Comprehensive Equipment and Utility Change Control for GMP Production Facilities
- Drug Development and Delivery: Biosimilar Biological Products: Development & Applications
- EASeNews: Top Five Hurdles for ANDA Submissions and Approvals
- ISPE: How GMPs and Data Integrity Align for Safer Products and Swifter Approvals
- ISPE: Pharma Industry Opportunities to Streamlined Approach to Innovations
- EASeNews: Pharma’s Problems with Data Integrity
- EASeNews: Challenges with Implementing Cleaning Validation
EAS Consulting Group, with our global network of over 150 independent consultants, assists clients in all phases of product development and marketing. From design and review of safety studies, preparation and submission of applications such as DMF, NDA, ANDA and IDE, EAS provides you peace of mind. Our expertise helps you to meet and exceed FDA expectations for safety and efficacy. Let us help you with your drug products and experience the difference that our respected team of experts delivers.
Put GMP Compliance in Your Pocket!
EAS’ handy Pharma GMP Pocket Guide includes regulations for 21 CFR 210, 21 CFR 211 and 21 CFR 11 for electronic signatures, all in an easy to reference pocket sized guide, perfect for the manufacturing floor. Find it on the EAS website.
Posted in Drugs.