IRISYS, INC.
(858) 623-1520
8810 Rehco Rd Ste F
San Diego, California,
USA
92121-3262
irisys provides pharmaceutical product development contract services specializing in formulation development, cgmp manufacturing of clinical trial materials, pharmaceutical product development, dosage form development and consulting related to the drug development process.
- Annual Sales
- US$1 Million - US$2.5 Million
Products & Services
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- Irisys
- Dosage Form Development
- Pharmaceutical Product Development
- Pharmaceutical Dosage
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- Cgmp Manufacturing
- Formulation Development
- Drug Development
Web Result
- San Diego's Pharmaceutical Dosage Form and Drug Development Company - Irisys
- Pharmaceutical Dosage Form Development Company IriSys provides pharmaceutical product development contract services specializing in formulation development, tablet formulation, cGMP manufacturing of clinical trial materials, and consulting related to the drug development process. IriSys custom approach to drug development is supported by the Companys scientific and regulatory experience in movin...
- Why IriSys?
- CONTACT US | EVENTS | HOME Choosing IriSys for Dosage Form Development IriSys often works with companies that need to bring compounds to First in Man studies when the bioavailability is unknown and where there is limited stability data. These companies need to generate data in humans as early as possible to determine if the compound of interest is a candidate for further development. Company | Pre...
- San Diego's Pharmaceutical Dosage Form and Drug Development Company - Irisys
- Pharmaceutical Dosage Form Development Company IriSys provides pharmaceutical product development contract services specializing in formulation development, tablet formulation, cGMP manufacturing of clinical trial materials, and consulting related to the drug development process. IriSys custom approach to drug development is supported by the Companys scientific and regulatory experience in movin...
- cGMP Manufacturing Facility
- CONTACT US | EVENTS | HOME IriSys facility consists of 10,000 SF regulated by Standard Operating Procedures and current Good Manufacturing Practices. Three cGMP manufacturing suites accommodate lot sizes appropriate for Phase I and Phase II clinical trials. IriSys maintains a California Drug Manufacturers License. Company | Preclinical Development | cGMP Manufacturing | Platform Technologies | Reg...
- IriSys - Site Map for Pharmaceutical Dosage Form Development
- CONTACT US | EVENTS | HOME IriSys provides pharmaceutical product development contract services specializing in formulation development, cGMP manufacturing of clinical trial materials and consulting related to the drug development process. Our site offers information about cGMP manufacturing, dosage form development, drug development analysis, and more. COMPANY PRECLINICAL DEVELOPMENT cGMP MANUFAC...
Website Links:
IRISYS, INC. | Case Study IX: Topical... | Case Study X: Poor Solubility... | cGMP Manufacturing | cGMP Manufacturing Facility | Copyright Privacy | dosage form development | Drug Packaging | Formal Stability Studies | New drug development | pharaceutical formulation | Platform Technologies | Preclinical Development | Quality Assurance | Quality Control | Regulatory Affairs | Why IriSys?
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