Sikalia Pharmaceutical Laboratories
Sikalias Laboratories, established in 1967, is dedicated to producing high-tech pharmaceutical, nutritional, medical, and cosmetic products with a focus on safety, quality, and respect for pharmaceutical science. They utilize modern research and development facilities, GMP-compliant production lines, and adhere to strict quality control and environmental management standards to serve human health and meet international quality standards.
Industries
Nr. of Employees
small (1-50)
Sikalia Pharmaceutical Laboratories
Products
Oral liquid formulations
Oral liquid products manufactured at industrial scale under GMP conditions (client or in-house formulations).
Spray formulations
Spray dosage forms produced and packaged on-site under controlled environmental conditions.
Topical creams, emulsions and gels
External-use formulations (creams, emulsions, gels) manufactured and packaged in automated lines within controlled clean environments.
Oral liquid formulations
Oral liquid products manufactured at industrial scale under GMP conditions (client or in-house formulations).
Spray formulations
Spray dosage forms produced and packaged on-site under controlled environmental conditions.
Topical creams, emulsions and gels
External-use formulations (creams, emulsions, gels) manufactured and packaged in automated lines within controlled clean environments.
Services
Manufacture and packaging of client formulations across oral liquids, sprays and topical products on-site in GMP-certified facilities.
Custom product development including supplier selection, formulation, laboratory and pilot-scale batch production, method development and stability studies.
Preparation and submission support for product registration dossiers and regulatory approvals tailored to target distribution territories.
In-process, release and stability testing performed by trained analytical staff as part of QC operations.
Documented QA system implementation aligned with GMP and ISO standards, including internal audits and annual management reviews.
Manufacture and packaging of client formulations across oral liquids, sprays and topical products on-site in GMP-certified facilities.
Custom product development including supplier selection, formulation, laboratory and pilot-scale batch production, method development and stability studies.
Preparation and submission support for product registration dossiers and regulatory approvals tailored to target distribution territories.
In-process, release and stability testing performed by trained analytical staff as part of QC operations.
Documented QA system implementation aligned with GMP and ISO standards, including internal audits and annual management reviews.
Expertise Areas
- Contract manufacturing
- Formulation development and scale-up
- Quality control and analytical testing
- Quality assurance and ISO/GMP compliance
Key Technologies
- GMP manufacturing
- Automated production and packaging lines
- Laminar flow cleanroom arrangements
- HVAC environmental control (temperature, pressure, humidity)