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2320 Scientific Park Drive, Wilmington, NC, 28405, US
Alcami is a US contract development and manufacturing organization with 45+ years of experience advancing pharmaceuticals and biologics from development to delivery. Alcami provides fully integrated lab services, drug product manufacturing, and cGMP pharma storage and support services including calibration, validation and environmental monitoring.
As drug development grows increasingly complex, pharma and biotech teams are seeking partners with the scientific depth and agility to keep pace.
Released By Alcami Corporation
Precise storage conditions are critical to maintaining the quality and integrity of pharmaceutical products. Pharma storage must provide secure, cGMP-compliant solutions backed by advanced infrastructure, including redundant power and cooling systems, 24/7 monitoring, and multi-layered access control. A full spectrum of storage environments—from ambient, refrigerated, and ICH stability to ultra-low and cryogenic—are needed to meet […]
Timothy Compton of Alcami shares insight on Alcami's role in ensuring a smooth transition from development to manufacturing.
Gain insights into the parenteral and fill-finish manufacturing markets, opportunities, and recent investments in the space.
Chad Bovero, James Fife, and Tobin Cowart promoted to senior leadership team.
Alcami to manufacture PharmaTher’s proprietary ketamine products for FDA Phase 3 clinical studies and global commercialization.
A $31 million investment will expand its sterile development and manufacturing operation in Charleston, SC.
Alcami used a Gerteis Mini-Pactor® roller compactor to develop a capsule formulation and critical processing parameters at the target dosage in record time.
25-year industry professional brings a track record of leading high-performing, client-centered business teams.
WHO, FDA and the European Pharmacopoeia have established strict regulatory guidelines to guarantee product quality in biologics.
Due to the high costs and low demands of the drug product, it is important to efficiently use API supply during the formulation process.
In this webinar, Alcami’s Brent Harlow will guide you through the necessity of these studies and how to successfully perform them for FDA approval.
Sign up to get a close-up look at our US network of laboratories and hear about our expansion plans.
The agreement represents another step toward the proprietary manufacturing, formulation, and delivery of products for Tryp’s PFNTM program.
He succeeds Walter J. Kaczmarek III, who is stepping down as Chief Executive Officer.
Formulation and Method Development.
Parenteral Forms.
Wether you are a virtual start-up or a large organization, you and your patients deserve subject matter experts who take ownership of your program from clinical trals through commerical supply. Partnering with Alcami as your contract development and manufacturing organization connects you to a US-based team of dedicated professionals with over 40 years experience advancing […]
Emerging Technology Needs and Value Proposition for Strategic Partnerships with Contract Development and Manufacturing Organizations (CDMOs)
Alcami, a leading United States-based contract development and manufacturing organization (CDMO), announced an additional $2 million investment to expand its oral solid development and manufacturing capabilities in Wilmington, NC. The investment will add a Gerteis Mini-Pactor® roller compactor and low humidity suites to Alcami’s existing 140,000 square foot campus in Wilmington, NC. The expansion, which is on track to be completed in the first […]
High-resolution mass spectrometry is a key component in the characterization of novel biologics and biosimilars.
Alternate methods of administering solid oral formulations are necessary to meet the needs of all patients.
by Chris Williams, Julia Spraul (pictured), and Alyssa McBurney
Will evaluate Cellares’ fully automated, high-throughput manufacturing platform in preparation for expansion into new indications.
By: Charlie Sternberg
Designed to improve analytical capabilities by separating particles prior to analysis, enabling high-resolution characterization.
By: Kristin Brooks
Introduces Simplist Ephedrine Sulfate Injection, USP and Simplist Succinylcholine Chloride Injection, USP.
The collaboration will leverage AGC Biologics' mRNA manufacturing knowledge and expertise to combat a leading cause of human mortality.
Save your seat for Contract Pharma's December 9th webinar with USP.
Released By U.S. Pharmacopeia (USP)
Dr. Vor der Brüggen ascends to this new role after several years leading Schreiner Group’s Research and Development segment.
Nelson Labs’ Christine Walton provides insights on newly proposed regulatory chapters.
Released By Nelson Laboratories, LLC
The trial tests PBGENE-HBV for patients with chronic Hepatitis B.
By: Rachel Klemovitch
The acquisition adds Durect's lead asset, larsucosterol, to Bausch Health’s hepatology pipeline.
As CDMOs prepare for the future, Ben Locwin examines regulatory shifts, technological advances, and talent challenges—and brings these insights as keynote speaker at Contract Pharma’s 2025 Conference & Expo in New Brunswick, NJ, Sept. 18-19.
By: Ben Locwin
Partnership aims to improve cell separation and increase cell viability.
The license for IXCHIQ was suspended based on four new reports of serious adverse events consistent with chikungunya-like illness.
Will leverage Andelyn’s suspension AAV Curator platform to provide scalable manufacturing of clinical-grade AAV material.
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