Company Overview
Skandanana Pharma Pvt Ltd.
Skandanana is experienced in pharmaceutical services, with experience in research laboratories, scale-up, clinical and final cGMP manufacturing, packaging and warehousing. Our expertise encompasses API, biologicals, OSD, inhalable, liquids, and aseptic processing as well as all aspects of equipment, containment and isolation, controls and conformance to the latest regulatory requirements. Skandanana is offering world class services to its clients in the fields of Turnkey Projects, Analytical Lab design, Software development
What we do ?
SPPL can assist, if a facility has existing processes in place, but a production line requires improvement through automation and Software integration, along with other enterprise systems.
Analytical Lab design
Our experienced specialists develop ‘state-of-the-art’ solutions for customers’ an analytical laboratories ...
Safety Projects
All safety projects will handle as per local and International standards of statutory fulfillment with a regulatory compliance approach establishment.
Turnkey Projects
Skandanana is a fastest emerging organisation in design, engineering and construction in the life ...
Project Validation Services
Project Validations services includes Facility Validation, Equipment Validation of process & laboratory, Utilities Validation
Consultancy and Auditing Services
Audits are needed in order to ensure compliance. To stay ahead of the curve, you need to remain audit-ready at all times...
Software Solutions & Development
Key advantages to using SPPL for your Automation Integration include our extensive experience ....
Why us?
Skandanana Pharma
Specialised in consultancy for new start-up of Pharma companies and support in the revamping of Existing Pharma companies in all disciplines of services for API, Excipients, solvents, R&D set-up and Formulation of various dosage forms.
Skandanana Pharma also handles turnkey Pharma projects, Software development & Validations, Supply of HVAC systems and Clean room Panels; where having a dedicated team to monitor the ongoing cum pipeline projects completions thereof. Our knowledge on the demands of regulatory authorities such as FDA and others, enables us to provide a comprehensive high-quality service to all users.
