Develop your products

CHEMINEAU, YOUR LABORATORY
FOR FORMULATION AND DEVELOPMENT

Laboratoires Chemineau works on medicines, medical devices, cosmetics, food supplements and more as a renowned development partner with a strong R&D team. We can undertake your projects in the areas of pharmaceutical development and innovation, family health products and hygiene care in liquid, semi-solid, spray and aerosol formats.

Laboratoires Chemineau operates within a dynamic ecosystem, meaning clients can use our experience and large network of experts to generate greater tangible benefits and added value.

Our agile R&D teams provide a full range of services:

  • Product innovation: for increased efficiency, practicality, agreeableness, adhesion and memorability; to solve stability problems, process reliability issues, etc.
  • Quality or regulatory monitoring and advice
  • Risk management: industrial and quality, procurement, etc.

DEVELOPMENT MODELS

Any development or innovation pathway is conceivable. We adapt to your needs, no matter your project’s level of maturity and complexity. Our teams are set up for projects and have a project manager. This means support from beginning to end; from design to launch, and provides the necessary convenience and responsiveness.

Laboratoires Chemineau offers different development services to meet varying needs:

  • Design :
    • Formulation
    • Eco-design
    • Sourcing
    • Dual sourcing
  • Development/Transposition:
    • Development
    • Analytical checks
    • Method and process development
    • Stability studies
    • Industrial transposition
    • Technology transfer/insourcing

We master the manufacture of clinical batches (experimental drugs and medical devices subject to clinical investigations), under GMP conditions.

Having worked on hundreds of development projects, we have acquired a solid skillset.

Ask us to resolve industrial, supply, quality and CSR challenges involving redevelopment work. We have the expertise to support you with procurement, eco-design, formulation and industrial process issues, and with researching formula and packaging solutions.

Chemineau will develop, produce and put together your regulatory dossier as soon as possible, no matter the product status.

Have an idea for a health product? A gut feeling? Laboratoires Chemineau is ready to listen and develop your product.

Whether you need to think about formulation, develop the production process or create a regulatory dossier, the Chemineau teams are here to help and make suggestions about how to meet your requirements in the shortest possible time.

LICENSED PRODUCT CATALOGUE

UPPER RESP. IMMUNITY

  • Prevention & relief of colds & influenza

NASAL RELIEF

  • Nasal Dryness Spray
  • Pollen & Pollution Catcher Nasal

NASAL CLEANSING

  • Isotonic Nasal Cleansing Spray
  • Hypertonic Nasal Decongestant Nasal Spray
  • Children Eucalyptus Decongestant Nasal Spray
  • 2 in 1 Decongestant and Soothing Nasal Spray
  • Relief of Sinusitis
  • Fluidifying Nasal Cleansing Spray (medicine)

NASAL DECONGESTANT

  • Potent Essential Oils & Hyaluronan Nasal Spray

SORE THROAT RELIEF

  • Multi-Symptom Sore Throat Relief Spray
  • Anesthesic and Antiseptic Throat Spray (medicine)

  • Arnica Topical Gel
  • Fast acting CBD Microgel
  • Diclofenac 1% Gel & Foam (medicine)
  • Ibuprofen 5% Gel (medicine)

  • Hygiene & Care for Acne
  • Hygiene & Care for Psoriasis
  • Econazole 1% Cream & Power (medicine)

BABY CARE

  • Baby Nappy Rash Liniment

WOMEN’S HEALTH

  • Lubricant Intimate Gel
  • Heavy Legs Topical Gel
  • Night-Time Sleep & Menopause Aid Liquid

SLEEP

  • Night-Time Sleep & Stress Aid Liquid

Register and download the Laboratoires Chemineau and ANJAC Group in-licensing catalogue at www.myprivateanjac.com

REGULATORY MONITORING AND ADVICE

Laboratoires Chemineau has the technical and regulatory expertise to provide:

  • End-to-end creation of MA dossiers for medicines and technical dossiers for medical devices;
  • Creation of cosmetic dossiers, an area of ANJAC Group expertise;
  • Maintenance of your authorisations and certifications;
  • Variations (IIA, IIB, III);
  • Renewals
  • Responses to authorities
  • Clinical batch supply;
  • Medical and scientific support with any questions;
  • Dossier submission to authorities;