Dermatology industry / Cosmetics

contact

print

Drug Formulation services

NUVISAN has acquired  in 2018 the Sophia Antipolis Site, which was the flagship of Galderma’s Research and Development in Europe. Through this NUVISAN gained and developed the topical drug development expertise, from Formulation development to Manufacturing, packaging and distribution.

Our team or 20 scientists has years of experience and is able to develop and test scaffolds with the objective of creating and/or developing creams, ointments and oils top the parameters needed.

The associated analytical and chemical services are highly supportive in assessing the objectives and fine-tuning through physical and/or chemical properties, which is a unique asset in today’s industry.

Please review our services here

Chemical Synthesis

Our chemical synthesis process development - to GMP batch production will support the topical formulation development by measuring and improving the drug product while joining its forces with the drug substance unit. Our ability to assess for polymorphism and work around the chemistry is not only unique in the offer but also a great shortcut in creating more value, faster.

Please review our services here

Clinical Trial Supply services

NUVISAN can support the whole process from manufacturing to primary and secondary packaging.

With dispatch sites available in Germany and France, and a network of depots across the globe our team is here to guarantees efficient logistics to your clinical trial sites, wherever they are located.

Please review our services here

Non-Clinical testing

Drug delivery and safety assessment is essential to the preclinical stage of your development.

Whatever route of application you need to develop, from fully open applications to fully occlusive our teams will be here to bring solutions.

NUVISAN provides all necessary models, in vitro and in vivo to help understand and develop further the efficiency of your topical drug, with the complete bioanalytical platform to support.

Please review our services here

Clinical Development

We can develop and assess the kinetics, comparative safety and efficacy of your topical drugs.

Our clinal facilities located in Germany (Neu Ulm and Gauting) have a solid experience in preforming trials for drugs delivered through the topical route.

In the same way as for clinical development NUVISAN provides all bioanalytical support to further support your developments.

Please review our services here

Related Topics

close

This service is only available in the desktop version.

Our Services & Solutions along
the Drug Development Value Chain

Please click and choose a category

Discovery

PRECLINICAL

Clinical Phase I

Clinical Phase II

Overall Services

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management