Purpose-Driven Products

At Wilcrest Pharma, we’re committed to partnering with healthcare organizations to provide solutions for the most challenging compounded medications. Our product development pipeline hinges on a foundational expertise in clinical and technical formulation creation, supported by the ability to bring products to market quickly in a CGMP-compliant environment.

Become A Customer

How We Serve Our Customers

Oncology

Remove complexity from your workflow with ready-to-use, CGMP antineoplastic medication

Cardiology

Simplify treatment with solutions built to fit smoothly into your clinical routine

ENT

Minimize prep, maximize control with medications developed with providers and patients in mind

Transplant

Temperature-stable medication designed to integrate into immunosuppressive protocols where therapeutic control is essential

Custom Products

Wilcrest’s focus on unmet needs allows us to have conversations centered around product developments that make a difference in the lives of your providers and patients

Contact Development Manufacturing

Organizations seeking contract manufacturing opportunities with Wilcrest can be confident in a relationship that will prioritize your patient needs, from formulation research to product release

Account registration and ordering process

Wilcrest Pharma is focused on developing lasting relationships that start with crucial conversations on your patients’ needs. Our team is ready to take on your toughest formulations.

Become A Customer

Step 1: Register For Account

Step 2: Hear from Our Team

Step 3: Place Your Order

Our Innovation Engine

Identification

Collaborate with providers to understand therapeutic goals, patient demographics, and delivery preferences. Define intended use, target dosage forms, route of administration, and relevant clinical context.

Formulation Research

Explore formulation needs to address stability, solubility, or preservative-free requirements. Identify suitable container-closure systems and perform risk assessments, as applicable and needed.

Development

Supply chain considerations, understanding batch yields, staffing needs, production planning, and equipment qualifications. Planning and executing Phase I testing- microbial and analytical method validation.

Pilot Batches & Validation

Planning and executing Phase II testing- validation of storage conditions and beyond-use-dating. Triplicate pilot batch runs to simulate full-scale production. Finalizing quality specifications for product release and environmental monitoring.

Release

Begin production, third-party quality testing, visual inspection, labeling, batch disposition, final release, and order fulfillment.