Join Bikash Chatterjee, tomorrow at 11:35 AM for a panel discussion on Driving Next-Gen Biomanufacturing with Digital Transformation. With his fellow panelists, he’ll be exploring how digital transformation is essential in helping improve product quality.

See you tomorrow at CPHI Milan in Milan, Italy! We’re excited to meet up with everyone again this year. Stop by Booth 4C113 and let’s talk about we can help you navigate the complexities of bringing your drug to market.

Join the Pharmatech Associates team next week at CPHI Milan in Milan, Italy from Oct. 8 – 10! Find us at Booth 4C113 of set up time to meet about your next project here: [email protected]

Attending CPHI Milan October 8 - 10? If so, let’s talk drug development, quality, and the complexities of regulatory filings! Visit us at Booth 4C113. hubs.ly/Q02Ql9lQ0

Join tomorrow’s webinar on PCM for Drug Substance (API) on Sept 26th, 2024 at 11:00 AM EDT! Learn about PCM principles, technologies, and challenges. Register here now: hubs.ly/Q02Qlw070 #PCM #Pharma #ContinuousManufacturing

Join us tomorrow for an insightful webinar on entering the US drug market at 11:00 AM EDT. We’ll cover portfolio analysis, CDER’s quality practices, and more. Register here now: hubs.ly/Q02Qlmzs0 #USPharmaMarket #DrugDevelopment

Overcome challenges in PCM for Drug Substance! Join our experts on Sept 26th at 11:00 AM EDT to navigate PCM implementation hurdles. Sign up here: hubs.ly/Q02QlqWV0 #PCM #Pharma #ContinuousManufacturing

Ready to expand into the U.S. drug market? Join our webinar on 9/25/2024 at 11:00 AM EDT to learn about portfolio analysis, CDER’s quality practices, and commercial readiness. Register today: hubs.ly/Q02Qlddm0 #PharmaIndustry #DrugDevelopment

We’re 3 weeks away from CPHI Milan and we can’t wait! Join Bikash Chatterjee at two panel discussions – on Oct. 8 and 9. We’re looking forward to seeing everyone there! Register Here: hubs.ly/Q02QkRqY0

Join us for a comprehensive webinar on PCM for Drug Substance on Sept 26th at 11:00 AM EDT. Discover PCM trends, technologies, and business cases. Register now: hubs.ly/Q02Qld8L0 #PCM #Pharmaceuticals

Don't miss our webinar on 9/25/2024 at 11:00 AM EDT! Learn about the essential steps for U.S. drug market entry, from FDA filings to quality management. Register now: hubs.ly/Q02QlmNw0 #Pharmaceuticals #RegulatoryAffairs

Unlock the potential of PCM for Drug Substance! Join us on Sept 26th at 11:00 AM EDT to explore PCM technologies and business cases. Register today: hubs.ly/Q02N2bRM0 #PCM #Pharma #ContinuousManufacturing

Attending the PDA/FDA Joint Regulatory Conference 2024 in Washington, DC Sept. 9 – 11? Join us at the Westin Washington, DC Downtown. Visit the Pharmatech team at Booth 111 and let’s talk about quality and CGMP. Register here: hubs.ly/Q02KJBG90

Excited to announce our webinar on 9/25/2024 at 11:00 AM EDT on Entering the U.S. Drug Market! We’ll cover product portfolio analysis, regulatory submissions, and more. Don't miss out! Register here: hubs.ly/Q02LP7Rr0 #Pharmaceuticals

Don't miss our PCM for Drug Substance webinar! Discover the current PCM DS landscape and overcome adoption challenges on Sept 26th at 11:00 AM EDT. Sign up here: hubs.ly/Q02Lw0Cn0 #PCM #Pharmaceuticals

Ready to expand into the U.S. market? Join our webinar on 9/25/2024 at 11:00 AM EDT to learn which products to pursue, CDER’s quality practices, and get insight into commercial readiness. Register today: 1. hubs.ly/Q02LPfcn0 #DrugDevelopment

The PDA/FDA Joint Regulatory Conference 2024 in Washington, DC is happening Sept. 9 – 11 at the Westin Washington, DC Downtown. It’s focused on Current Good Manufacturing Practice (CGMP): Leading with Quality and Integrity. Visit us at Booth 111! Register: hubs.ly/Q02KJx9h0

Some of the team gathered for a day of fun at a local California vineyard and philanthropy to support Ronald McDonald House-a San Francisco Bay location that supports families with local housing while their children are receiving life-saving medical treatments.

There are some challenges in the U.S. generics market such as finding reliable distribution partners and maintaining data integrity. Each one of these steps requires strategic planning and a deep understanding of regulatory landscapes. #GenericDrugs hubs.ly/Q02zMvnb0

Our clinical and #regulatoryaffairs team has extensive experience with small compounds, cell and gene therapies, and biologics. We design thorough regulatory plans that guarantee the creation, assessment, and marketing of successful products. hubs.ly/Q02zMvgz0