Allay Pharmaceuticals, LLC. has been helping pharmaceutical companies worldwide, bringing products to market - from concept to commercialization, assisting every step of the way.

We are your reliable outsourcing partner for quality and affordable product development, analytical services, regulatory and compliance support, as well as other technical services. Whether you need a stand alone service or a combination of services, we can provide the solution that best fits your need.

Our most valued asset is our proficient specialists, whose combined expertise encompasses all aspects of pharmaceutical development and operations. The experience profile of our scientists range from 15-35 years with over 250 ANDA approvals and hundreds of successful formulations of NCEs developed and cGMP Clinical Trial Materials manufactured.

Our regulatory and compliance support services include but not limited to, filing of INDs, NDAs, ANDA, resolution of FDA deficiencies and site pre-approval inspection readiness. We serve a diverse group of clientèle globally as regulatory agents, to assist with registration of their facilities and their products with US FDA and foreign Health Ministries. Our Technical Service Group provide on-site services to resolve manufacturing process issues and consultation for qualification of equipment and laboratory instruments.

Our facility, registered with the Food and Drug Administration (FDA) is operated under current Good Manufacturing Practices (cGMPs) and an independent Quality Assurance program.

We are confident that we can solve your most complex drug development needs within a reletaively short period. We strive to deliver excellence in customer satisfaction. We hope to have the opportunity to provide: the service that you need, with a target to achieve the desired outcome with maximum efficiency and accuracy.