What We Do
Commitment to Innovation
Our company understands the technology and medicine in the health care industry is consistently progressing. Our team of experienced professionals stays current about the latest drug trends.
Drug Development and Testing
Our team is constantly keeping up with medical trends and technology and strive to find better ways to improve the health of our patients in an ever-changing industry.
SERVICES
Active Pharmaceutical Ingredients
The Active Pharmaceutical Ingredient (API) is the part of any drug that produces the intended effects.
Custom services include:
- Custom synthesis of Active Pharmaceutical Ingredients and advanced intermediates
- Process development/scale-up
- Process validation
- Stability testing
- Test method development and validation
- Clinical Trial Material (CTM) and supporting documentation
- Drug Master File (DMF) development and maintenance
Working closely with clients ranging from virtual pharmaceutical companies to the world’s largest multinational pharmaceutical and biopharmaceutical producers, we synthesize proprietary and commercial compounds in quantities ranging from grams to kg.
Key product technologies:
High Potency Substance manufacturing in a certified development and commercial scale multi-purpose containment chemistry manufacturing facility
Sterile Injectable Grade Lactate salt solutions
In everything we do, motivated by a concern for both product quality and environmental /worker safety. We design and equip our plant, write our procedures and train our people to meet or exceed stringent regulatory protocols and international regulatory and multi-compendial standards.
API Process development
MM Pharma now has the technology and experience to offer you synthetic and semi-synthetic process development. No matter how simple or complex your API development needs may be we have the flexibility to customize our proven synthetic and organic process development services to meet your exact needs
Our experienced team of chemists can:
- Assist you in identifying new, potentially more efficient synthetic routes
- Reproduce your dynamic process veritably
- We do optimize, improve, refine your existing synthetic process to be both flexible and portable with its manufacturing schemes and regulatory strategies
- MM Pharma ensures that your drug substance will be made efficiently using cost effective processes. We test and validate your API in one of our manufacturing facilities or isolated GMP suites to make sure it can be scaled up using the synthetic process we develop for you.
- All of our routes are designed to be conducted in standard equipment using reliable and proven manufacturing methods to make it easy and convenient for you to transfer the production to another API supplier as your needs grow.
Process Technology Transfer
- Process development
- Scale up – engineering / safety
- cGMP API / HPAPI manufacturing
- Quality control
- Quality assurance
- Dedicated project management
PRODUCTS
Product Name
KETOROLAC TROMETHAMINE
PRUCALOPRIDE SUCCINATE
LINEZOLID
LEVOCETIRIZINE DI HYDROCHLORIDE
CARVEDILOL
RACECADOTRIL
AMISULPRIDE
TIZANIDINE HYDROCHLORIDE
RIVAROXABAN
BRIMONIDINE TARTRATE
HYDROXYZINE HYDROCHLORIDE
MOSAPRIDE CITRATE DIHYDRATE
MECLIZINE HYDROCHLORIDE
PREGABALIN
DAPOXETINE HYDROCHLORIDE
BILASTINE
ITOPRIDE HYDROCHLORIDE
DEFERASIROX
APIXABAN
Dapagliflozin
Modafinil
Iron Sucrose