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Solas Research & Development
Scientific innovation for sustainable health
We combine science, technology and empathy to bring trusted pharmaceutical solutions to the community.
5
R&D Formulator
Guiding formulation from concept to production validation.
4
R&D Researcher
Focus on active ingredient studies, pharmacology data, and clinical literacy.
5
Active laboratories
R&D instruments, formulation, furnace, stability, and QC with analytical sub-units.
PT. Solas Langgeng Sejahtera is committed to presenting safe and effective products through in-depth research. R&D is the foundation of every innovation, starting from selecting raw materials, exploring formulas, to validating product sustainability.
Close collaboration between the R&D and Quality Control teams ensures that every process follows Good Manufacturing Practice (GMP) standards. Stability testing, raw material analysis and quality monitoring are carried out continuously.
Currently there are dozens of active projects at various stages—from literature studies to production scaling—being carried out in parallel by our formulators and researchers.
The production facility is equipped with a modern laboratory with analytical tools that support measurable and documented research, so that every health solution we present has a real impact on society.
Main Focus
Formula Research
Developing stable, effective compositions suited to patient needs.
Validation & Stability Testing
Each batch undergoes temperature, humidity, and packaging compatibility testing.
Regulatory & Production Scale
Complete GMP documentation to mass production readiness.
Laboratory Facilities
Measurable research infrastructure
The QC lab has several sub-units (analytics, microbiology, and packaging testing) that ensure each batch meets quality standards.
R&D Process
Structured research stages
Each stage is protected by thorough protocols and documentation to ensure consistent and accountable results.
01
Needs discovery
Identifying patient needs and new therapy opportunities with healthcare professionals.
02
Active ingredient research
Selection of raw materials and suppliers that meet international pharmaceutical standards.
03
Formulation & prototype
Composing initial formula, organoleptic testing, and accelerated stability testing.
04
Scaling & validation
Ensuring consistent production processes when moving from lab to factory.
