Drug Substance to Drug Product
Pharmaceutical Development Consulting
From the qualification of your drug substance to the industrialization of your drug product, DS2DP-Consult supports you throughout the complete lifecycle of your development.
About us
25 years of experience at your service.
After more than 25 years in the pharmaceutical industry, I founded DS2DP-Consult based on a simple conviction: pharmaceutical development must remain focused on the patient—free from unnecessary complexity—while always prioritizing the drug’s efficacy and safety..
“Keep it simple for patient priority”
Multidisciplinary skills
Our areas of expertise
We support your pharmaceutical projects from raw material qualification through to registration of the drug Product, taking advantage of our recognized expertise in analytical and pharmaceutical development, process optimization, and CMC aspects.
We securize your methods, data, and transfers to accelerate every key stage of your development.
Your product moves forward with clarity, rigor, and compliance.
Pharmaceutical Development
Formulation improvement
API assessment and qualification
Evaluation of finished products
Supplier selection
Analytical developement
Methods Life Cycle Management
Method development
Method Validation
Multi-sites Analytical coordination
Analytical transfer
Packaging development
Packaging choice
Development plan
Combination products
Optimisation
Packaging process
Manufacturing process
Troubleshooting
Method harmonization
Impurity qualification
Large scale expertises
A wide technical scope offering services
You need to mitigate risks, harmonize practices, or ensure sound decision-making within a complex scientific and regulatory environment.
Your challenge lies not only in developing a product but also in ensuring it is qualified, controlled, compliant, and ready for registration.
Which areas do you need targeted support?
How can DS2DP-Consult help you turn operational constraints into drivers of performance?
API
High Potent Molecules
Formulation
Gels, caps, tablets, injectables
Packaging
Sachets, metering pumps, tubes, bottles, blisters pack
Routes
Topiques, orales, vaginales
A variety of experiences
key achievements
- Development and validation of stability indicating analytical methods
- Coordination of intercontinental analytical transfers
- Registration, renewing, and extending regulatory authorizations
- Support for CEP and DMF approvals
- Market maintenance for special status finished product
- Deployment of analytical laboratories
