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Business Details
23 Years
experience
Expert Drug Formulation Services in San Diego
Since 2003, Latitude Pharmaceuticals has established itself as a leader in pharmaceutical formulation development, completing over 900 projects for 250+ global clients. Our expertise lies in solving complex drug formulation challenges through innovative solutions like CLEARSOL, a novel vehicle for solubilizing difficult APIs. We combine deep technical knowledge with rapid turnaround times to deliver reliable, client-focused results. Our GLP/GMP-compliant manufacturing and analytical testing services support clients from formulation development through clinical trial material production.

With a worldwide reputation for creativity and client satisfaction, we provide end-to-end support for drug delivery systems. Our team's extensive experience ensures regulatory compliance and successful formulations, reducing development risks for biotech and pharmaceutical partners. Latitude's internal product development focuses on addressing unmet medical needs through improved drug formulations eligible for fast-track FDA approval pathways.
Services
Formulation Development GLP/GMP Manufacturing CLEARSOL Technology Analytical Testing Drug Delivery Systems
Details
  • Year established: 2003
Highlights and features
  • We have completed over 900 pharmaceutical formulation projects since 2003
  • Our team offers rapid turnaround times for drug formulation development
  • We specialize in GLP/GMP-compliant manufacturing for clinical trial materials
  • Our CLEARSOL technology improves solubility for difficult APIs
  • We provide end-to-end support from formulation to regulatory filing
Services
Formulation Development
We specialize in developing complex drug formulations for challenging APIs, leveraging 20+ years of experience with 900+ successful projects. Our expertise reduces development time and risk while improving solubility and stability. We support clients from preclinical through clinical stages with customized solutions.
GLP/GMP Manufacturing
Our GLP/GMP-compliant manufacturing services produce clinical trial materials meeting strict regulatory standards. We ensure quality control from formulation through final product release, supporting fast-track FDA approval pathways for improved drug formulations.
CLEARSOL Technology
CLEARSOL is a patented vehicle for solubilizing difficult APIs, forming stable aqueous solutions. This clinically-tested technology improves solubility beyond traditional methods while maintaining safety across multiple administration routes.
Analytical Testing
We provide comprehensive analytical testing services to validate formulation integrity and stability. Our capabilities include method development, validation, and release testing for clinical materials under GLP/GMP compliance.
Drug Delivery Systems
Our team develops novel drug delivery formats including intravenous, intramuscular, and extended-release formulations. These innovations address unmet medical needs while improving safety, stability, and ease-of-use for existing drugs.
Questions
What pharmaceutical services does Latitude offer?
We provide formulation development, GLP/GMP manufacturing, analytical testing, and drug delivery system innovation for biotech and pharmaceutical companies.
What is CLEARSOL technology used for?
CLEARSOL improves solubility for difficult APIs, forming stable aqueous solutions with better performance than traditional methods like cyclodextrins.
Does Latitude work with global clients?
Yes, we serve biotech and pharmaceutical companies worldwide with formulation development and manufacturing services.
Can Latitude help with FDA approval?
Our formulations support fast-track 505(b)(2) NDA pathways, reducing time and costs for FDA approval.
What makes Latitude different from competitors?
With 900+ projects since 2003, we combine rapid turnaround times with innovative solutions like patented CLEARSOL technology for complex formulation challenges.
Do you offer sample testing for CLEARSOL?
Yes, we provide free CLEARSOL evaluation samples for clients to test API solubility in their own laboratories.