Pharmaceutical formulation development
Success in the pharmaceutical sector starts long before a product is put on the market. It begins in the laboratory, where, via the critical process of pharmaceutical formulation development, concepts are transformed into actual, stable, and effective medications. Delivering R&D-driven formulation development services that satisfy international regulatory and quality standards is our area of expertise at Salvavidas Pharmaceutical.
Our scientific experience guarantees that your product is safe, effective, and prepared for commercialization, whether you’re creating a new medication, altering an old formulation, or getting ready to enter foreign markets.
Pharmaceutical Formulation Development: What Is It?
The process of turning an active pharmaceutical ingredient (API) into a consumable dosage form—such as a tablet, capsule, injection, syrup, or cream—is known as pharmaceutical formulation development. This includes:
- Choosing the appropriate excipients
- Maintaining the stability and bioavailability of drugs
- Improving the distribution technique, taste, and appearance
- Testing for performance and compatibility
It’s the intersection of science and accuracy that produces medications with reliable therapeutic effects.
The Significance of Formulation Development
Excellent medication concepts are only as good as how they are presented. Without the proper wording:
- The API may deteriorate or lose its effectiveness.
- The body may not adequately absorb the medication.
- The dosing form could not be appetizing or steady.
- Patient safety and compliance may be in jeopardy.
Formulation essentially fills the gap between market success and discovery.
Salvavidas Pharma: A Reliable Partner in the Development of Pharmaceutical Formulations
Comprehensive formulation development services catered to your molecule, market, and regulatory environment are provided by Salvavidas Pharmaceutical. From initial feasibility to pilot-scale manufacturing, our in-house R&D team and state-of-the-art labs offer innovative solutions.
In both domestic and foreign markets, we support customers in the branded, generic, nutraceutical, and over-the-counter sectors.
Our Fundamental Skills in Formulation Development
1. Studies on Preformulation
- Physical and chemical description of APIs
- Analysis of solubility, pH, hygroscopicity, and stability
- Excipient compatibility studies
2. Prototype Formulation Development
- Design of experiment (DoE)
- Excipient Selection and Optimization
- Production of small batches
3. Analytical Methods Development
- HPLC/UV/IR technique validation
- Stability-indicating methods
- Impurity Profiling
4. Testing for Stability
- Long-term and expedited stability studies
- Storage conditions that comply with ICH
- Prediction of shelf life
5. Scale-Up and Technology Transfer:
- Pilot-scale manufacturing.
- Process validation and documentation
- Smooth transition to commercial production
Forms of Dosage We Create
Our group has worked with a broad range of dose forms:
- Oral solids (powders, granules, pills, and capsules)
- liquids used orally (syrups, suspensions)
- Parenterals (vials, ampoules, and injectables)
- Topicals: gels, ointments, and creams
- Nutraceuticals (chewable pills, herbal supplements)
Every formulation is made to optimize market success, patient compliance, and bioavailability.
Who Requires Services for Formulation Development?
Our offerings are perfect for:
- Pharmaceutical firms introducing novel compounds to the market
- Formulations are changed by generic businesses to improve performance.
- Exporters who want formulas that adhere to national regulations
- Healthcare companies creating wellness or nutraceutical products
From lab bench to pharmacy shelf, we assist you in bringing your idea to life.
The R&D Infrastructure of Salvavidas
The Department of Scientific and Industrial Research (DSIR) has authorized our state-of-the-art research and development facility. It has the following features:
- Completely furnished analytical laboratories
- distinct formulation laboratories for injectable, liquid, and solid doses
- ICH Zone II and IV stability chambers for testing
- Systems for managing data for compliance and documentation
Regulatory Support for Every Project
Formulation is only the beginning. We also help with:
- CTD and ACTD dossier preparation.
- BE/BA Study Design Support
- Packaging and labelling compliance
- Regulatory Submission Documents
We understand the complex global regulations and make sure your product is ready for FDA, EU, WHO, and other government reviews.
Why Use Salvavidas for Formulation Development?
Here’s why international pharmaceutical companies trust us:
- 🧪 Expert scientists with decades of formulation experience.
- đź“Š Excellent analytical and regulatory paperwork support.
- 🧼 GMP-compliant pilot and commercial facilities.
- 🚀 Quick turnaround from concept to commercialization.
Let's innovate together.
Your formulation serves as the foundation for your pharmaceutical brand. Let Salvavidas assist you in creating it with precision, enthusiasm, and compliance.
đź“ž Contact us immediately to discuss your idea or book an R&D consultation.
📧 Get experienced advice, consistent results, and a partner who cares about your success.
Salvavidas does more than only produce treatments; it also builds trust.
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