ICYMI: Pace® Life Sciences acquired a laboratory facility in Lebanon, New Jersey, and expands FDA-registered central laboratory services. Eric Roman, CEO of Pace® said “This acquisition builds upon our leadership in the analytical services space to support emerging drug development partners through commercialization activities. I am excited to leverage this expansion with the New Jersey team to further collaborate with our pharma and biopharma clients.” Read more here: https://ow.ly/Q4KG50SAF07
About us
Pace® makes the world a safer, healthier place. Pace® People are committed to advancing the science of our customers in the pharmaceutical and biopharmaceutical industries. Pace® Life Sciences provides a full suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries from our network of CDMO sites, GMP analytical testing laboratories, and manufacturing support service centers. Our experienced, highly trained industry experts, and our investment in state-of-the-art development and manufacturing facilities emphasizes our commitment to efficiently advancing client programs through the clinic to commercialization. We are dedicated to delivering the best and most reliable services with positive customer experiences across all channels of our business. A subsidiary of Pace® Science and Technology Company, Pace® Life Sciences operates a network of multiple CDMO sites, FDA-registered GMP analytical testing laboratories, and regulatory and manufacturing support service centers across the United States.
- Website
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https://www.pacelabs.com/life-sciences.html
External link for Pace® Life Sciences
- Industry
- Pharmaceutical Manufacturing
- Company size
- 501-1,000 employees
- Headquarters
- Oakdale, Minnesota
- Type
- Privately Held
- Specialties
- Drug Development, Formulation Develoment, Analytical Method Development, Small Molecules, Nucleic Acids, CMC Analytical Services, Biologics, Hybrids, Pharmaceutical Development Services, Biopharmaceuticals, Lyophilization, Preclinical Development, Stability Testing, Solubility Enhancement, Solid Oral Dosage Forms, Parenterals, Ophthalmics, ADCs, Antibodies, Solid Form Development, RNA, Spray Drying, Preformulation , Microbiology , Extractables/Leachables, Finished Product Testing , Gene Therapy, Oligonucleotides, Clinical Trial Materials Manufacturing, Test Article Preparation, ICH Stability Programs, Raw Materials Clearance Programs, In-process & Finished Product Testing , Reference Standard Programs, Extractables-Leachables, Microbiology, GMP Laboratory Testing , CMC Pharmaceutical Development, Pharmaceutical Development, GMP Clinical Trial Material Manufacturing, Staffing/Insourcing, Regulatory Support, Instrument Services , Laboratory Relocations, Calibration & Mapping, Cleanroom & Pharmacy Testing, Service Plans , Hazard Communication, Raw Material Data Management , Product Stewardship, and FDA Regulatory Consulting
Locations
Employees at Pace® Life Sciences
Updates
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The first two installments of the Navigating the FDA Regulatory Roadmap Webinar Series are available to view on-demand. Don't miss Paula Garcia Calavia, Ph.D. with "The Investigational New Drug Application (IND) Process," and Darius J. Devlin, Ph.D. with "Obtaining Orphan Drug Designations for Rare Disease Treatments." You can view the Investigational New Drug Application (IND) Webinar here, https://ow.ly/bgYC50SCxvr You can view the Orphan Drug Designation Webinar here, https://ow.ly/I5bs50SCxB8 #drugdevelopment #lifesciences #webinar #regulatory #pharma #FDA #EMA #orphandiseases #orphandrugs #regulatoryaffairs #clinicaltrials
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"Developers targeting infectious diseases with new antibiotic solutions will find essential guidance in our FDA Qualified Infectious Disease Product (QIDP) Designation White Paper. This guide offers a deep dive into combating antibiotic resistance through the QIDP designation, detailing both the application process and the strategic benefits. Download it now to equip yourself with the knowledge to navigate this pathway effectively: https://ow.ly/RoCY50SAys5 "
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Reflecting on our recent #FDA audit, Rosalind Acosta-Seda, Quality Manager, advises, “It is very important that the attitude is positive where the audit takes place and the process of providing objective evidence is organized. This confidence assures the inspector.” When interacting with regulators, be sure to cultivate the proper environment. She continues, “Documents must be provided in a timely manner to demonstrate control and organization. All documents must be reviewed to check correctness and completeness before being provided to the inspector.” See the full recap here: https://ow.ly/COHj50S8GGI
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Are you ready to meet the stringent demands of clinical trials while ensuring your drug products uphold the highest quality standards? We offer specialized clinical packaging, kitting, and labeling services that seamlessly bridge the gap from development to delivery. Our sophisticated solutions are meticulously designed to safeguard your products and facilitate their smooth transition into clinical settings. 🔗 Discover how now: https://ow.ly/jLSj50SAylo
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Bioanalytical method development requires optimizing sample preparation and liquid chromatography in tandem with mass spectrometry (LC-MS/MS) methods. Dive into the details by accessing our on-demand executive summary today. https://ow.ly/hst850SAxco #Bioanalytical #MethodDevelopment
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📢 ICYMI: The U.S. Department of Labor published the #FinalRule for #OSHA to better protect workers and first responders. Find more below and in their announcement: https://ow.ly/Tcpi50SplL1 If this change adds to your workload, consider partnering with our team for reliable services and insight expertise. Read more about our offering here: https://ow.ly/e7GQ50SplL2
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Navigate complex medical device packaging regulations with confidence. Our ISO 11607 compliant testing validates package integrity, functionality, and strength. Partner with us to ensure your device arrives sterile and ready for use. 👉 Learn more here: https://ow.ly/3h2750SuYNk #medicaldevicepackaging #sterilepackaging
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Water systems validation helps ensure you maintain a state of control within your facility. We help navigate critical quality attributes, establish adequate protocol, and perform validation. https://ow.ly/nBAQ50Sv1ij
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We aim to please, and our team members are what set us apart! #CustomerService is a top priority for any offering we provide, which is why this feedback means so much to us. 🥰 #CustomerCompliments https://ow.ly/OUw550Sqpbj
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