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Pharma Services Category of UQUIFA

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API Development

Analytical Method Development

GMP Manufacturing

Hydrogenation

Ozonolysis

Preformulation & Material Science

Process Development & Optimization

Reference Standard

Regulatory Affairs / Pharmacovigilance

Scale Up

Small Scale Batch

Stability Studies

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UQUIFA

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GMP Compliant Manufacturing

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Uquifa is a company of first choice in API and advanced intermediates. We can offer R & D and cGMP compliant manufacturing across two continents (America and Europe)

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Pharma Service: API Manufacturing

Category: GMP Manufacturing

Sub Category: Overview

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Process Development, Optimization & Transfer

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process development, validation, analytical method validation, working standard supply.

- Directory Listing

Pharma Service: API Manufacturing

Category: Process Development & Optimization

Sub Category: Overview

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Scale-Up from Pilot Plant to Commercial

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: API Manufacturing

Category: Scale Up

Sub Category: Overview

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Reference Standard Synthesis

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: API Manufacturing

Category: Reference Standard

Sub Category: Overview

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Impurity Profile Characterisation

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Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Impurity / Reference Standard

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Stability Studies

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: Analytical

Category: Stability Studies

Sub Category: Overview

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Analytical Method Validation

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Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: Analytical

Category: Analytical Method Development

Sub Category: Method Development and Validation

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Polymorphism Studies

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, Polymorphism Studies, analytical method validation, working standard supply or impurity

- Directory Listing

Pharma Service: API & Drug Product Development

Category: Preformulation & Material Science

Sub Category: Polymorph & Crystal Screening

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Regulatory Support and File Submission and Ma...

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- Service Details

Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

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Pharma Service: Sales, Marketing, Registration

Category: Regulatory Affairs / Pharmacovigilance

Sub Category: Spain

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Small Scale API/NCE Production

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- Service Details

UQUIFA has pilot plants al all three facilities in Spain and Mexico. These plants are located on FDA approved sites and the pilot plants in particular have been inspected and approved by the FDA for small scale API/NCE production

- Directory Listing

Pharma Service: API Manufacturing

Category: Small Scale Batch

Sub Category: Overview

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Ozonolysis

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- Service Details

Production units are designed to be flexible allowing many combinations of reactors, filters and dryers to be used to perform the same type of reactions that are conducted at industrial scale, reactions such as nitrations, ozonolysis, hydrogenations

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Pharma Service: API Manufacturing

Category: Ozonolysis

Sub Category: Overview

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Hydrogenation

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- Service Details

Production units are designed to be flexible allowing many combinations of reactors, filters and dryers to be used to perform the same type of reactions that are conducted at industrial scale, reactions such as nitrations, ozonolysis, hydrogenations

- Directory Listing

Pharma Service: API Manufacturing

Category: Hydrogenation

Sub Category: Overview

Pharma Services Category of UQUIFA

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