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CLINICAL RESEARCH
(PHASE I, II, III & IV) :
WHAT WE DO :
1. Project Management :
2. Clinical Trial Execution :
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Study Initiation
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Site Monitoring/Management
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Quality Control/Quality Assurance
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Project logistic handling
3. Data Management :
4. Training and Development :
STRENGTHS AND SKILLS :
1. Extensive network of hospitals and medical institutes
throughout India.
2. GCP trained clinical trial monitoring team.
3. Well-defined SOPs to comply with GCP.
4. Database of investigators in diversified therapeutic area.
5. Collaborative work with the prestigious Govt. Research
Institutes for NCE.
We assure you of
Quality, Commitment, Confidentiality & Transparency
Generic
Formulations :
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State-of-the art
facilities, which adhere to stringent specifications of cGMP and
TGA-Australia, MCC-South Africa approved.
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Production capacity of
Tablets 3,900 million / year, Capsules 150 million / year,
Liquids 6,000 kilo liters / year, Vials + Ampoules 168 million /
year.
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Capabilities to
produce dosage forms in sterile and general, covering all
therapeutic segments along with lyophilization facility.
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Isolated and dedicated
production facilities for Beta-Lactam, Cephalosporin, Rifampicin
dosage forms and Insulin.
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Qualified and
experienced technical team in the areas of manufacturing,
quality control, quality assurance, research and development,
for all range of products.
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Experienced
professionals and highly qualified management and staff, with
SAP ERP and Supply Chain Management in place.
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Inspected & approved
by USFDA for Fluoxetine and Ethambutol.
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US DMF / EDMF / COS
filed / under process for about 20 products.
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ISO 9002 / ISO 14000
certified Bulk Actives manufacturing facility, offering
facilities for "Contract Manufacturing”.
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Product range: Active
Pharmaceutical Ingredients
·
Anti-allergic,
Cardiovascular, Anti-diabetic, Disinfectants,
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CNS, NSAIDs, Anti-TB,
Gastrointestinal, Anti-histamines
Economic
Value of Strategic Alliance :
Contract
Manufacturing with Cadila Pharmaceuticals enables
Pharmaceutical
companies to:
q
Reliable supply of
quality products - Validated and approved processes and in
compliance with the registration file.
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Minimize investments
in capital-intensive facilities.
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Improve net earning and cash flow.
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Divert resources to
focus on their core competencies – R&D and marketing.
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All products are
analyzed and released by our quality control staff before
shipment.
Monitor and
optimize the timeliness of our delivery and keep it up to our
customer’s full satisfaction
Business
Opportunities And Strategic Alliance With Cadila :
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We offer contract
manufacturing of all dosage forms.
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Depending on your
needs, our services include purchasing of raw materials,
production, packaging and quality control.
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Through this flexible approach, we are able to integrate
perfectly into your supply chain for solid dosage forms.
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Looking forward to partnering for a mutually beneficial
working relationship and a strategic alliance. |
