Protocol Development and Tech Support Services Expanded
Based on customers’ increasing interest, Lancaster Labs has expanded its services in protocol development and technical support. Customers can rely on the team to assist with CMC FDA filing, regulatory consulting and early-stage partnering to determine project needs and solutions.
Working with customers from project beginning on their regulatory and method development needs, Protocol Development writes technical documents and gives technical support for the pharmaceutical and biopharmaceutical technical departments. Documents include validation/qualification/verification protocols, specification documents, method transfer and other miscellaneous study types of documents performed under GMP and GLP conditions.
Technical support includes help in defining project scope, troubleshooting project challenges and providing background information the technical team may need in order to develop technically sound methods of analysis.
For more information, contact group leader Cindy Eby, 717-656-2300.