Formulation Development

Formulation Development
Product Description

1. Experts in analytical chemistry, Pre- formulation, formulation and nutraceutical development and optimization, as well as analytical testing and development services.

2. Extensive experience working Specialty Complex Products, Potent Products  & variety of dosage forms.

3. Product Development with focus only on regulated markets like US, Europe, Canada, Australia, South Africa, WHO, etc.

4. Highly Experienced Formulation Development & Analytical Support team.
 
5. Six (06) times USFDA Audited and Accepted Analytical lab delivering world class services to more than 150 pharmaceutical companies.

6. Largest Resource for Ion Chromatography; Extractable & Leachable studies & USFDA Inspected In-vitro Bioequivalence studies.

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mKnal Global Solutions

  • IN
  • 2022
    On CPHI since
  • 1 - 24
    Employees
Company types
CMO/CDMO
Consultancy
Contract Research Organisation (CRO)
Contract Service
Generics/Biosimilars Manufacturer
Manufacturer/Innovator
Pharmaceutical company
Primary activities
Pharmaceutical Company (generic finished products)
View company profile
Categories
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Specifications
  • Model
    Research and Development
More specifications Fewer specifications

mKnal Global Solutions

  • IN
  • 2022
    On CPHI since
  • 1 - 24
    Employees
Company types
CMO/CDMO
Consultancy
Contract Research Organisation (CRO)
Contract Service
Generics/Biosimilars Manufacturer
Manufacturer/Innovator
Pharmaceutical company
Primary activities
Pharmaceutical Company (generic finished products)
View company profile

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mKnal Global Solutions resources (1)

  • mKnal Global Solutions Corporate Presentation

    Brochure mKnal Global Solutions Corporate Presentation

    A global pharmaceutical consulting company engaged in providing pharmaceutical services for regulated markets viz. Europe, USA, Canada, Australia, China, etc.

    The company is actively working on Formulation Development and Contract Manufacturing including Supply chain. The companies key experience has been in the clinical development (Bioequivalence and Clinical Trial), Medical & Scientific Writing, GxP Audits and Reviews, Regulatory Services, Pre-Clinical work and Veterinary Product Development