Siddhi Vinayaka Spechem Pvt Ltd is GMP practicing and ISO 9001-2008 Certified company. We are leading Manufacturer of fine Chemicals especially Pharmaceutical Intermediates, Products For Peptide Synthesis, Carbohydrates And Dietary Supplements. All products are developed and manufactured in house adhering to the Q7A GMP Guideline.
Our Company is located in the outskirts of Bangalore, India. Our Company manufactures products with highest quality standards under stringent Environment, Health and Safety norms. We feel privileged for being audited by multinational companies such as Hoffmann La Roche, Bachem AG etc.
Siddhi Vinayaka Spechem Pvt Ltd is GMP and ISO 9001-2015 Certified company. We are leading manufacturer of fine chemicals especially pharmaceutical intermediates, products for peptide synthesis, carbohydrates and dietary supplements. All products are developed and manufactured in house adhering to the Q7A GMP Guideline.
Our company is located in the outskirts of Bangalore, India. Our company manufactures products with highest quality standards under stringent Environment, Health and Safety norms.We feel privileged for being audited by multinational companies such as Hoffmann La Roche, Bachem AG, etc.
WHY US ?
As an ISO 9001:2015 Company we assure that maintains consistent high standards. Svspl is committed to providing its customers with superior quality products and has implemented rigorous quality system to assure this.We place strong emphasis on quality parameters suggested by our esteemed clientele and work towards incorporating superior quality into our products and Processes.
By including customers in this process, we are able to prioritize their requirements. All our products are manufactured to clientâ€™s specifications and undergo testing to assure conformance. Additional test verifications are included to assure compliance with unique industry and customer specifications.
We believe that nothing short of top quality and consistency would satisfy our customers.
Consequently, we encourage our clients to give us as much feedback as possible, and over the years, we have formalized a process for reviewing this valuable input to find solutions. We promote continuous improvements in all the fields of activity through precisely defined Objectives, measurable indicators and process directed management system.
Some of the key factors that have helped us thrive in this competitive market are:
Develop and evaluate Product/Market Matrices for each.
we are focused on continually improving the way we do business; on operating with transparency in everything we do; and on listening to the views of all of the people involved in decisions.
We are higher growth trajectory and emerge stronger in terms of its global reach and in its capabilities in drug development and manufacturing.
Winning with Value Breakthrough Strategies for Market Dominance.
Planning for a sustainable competitive advantage
We focus on increasing the momentum in the generics business
ENVIRONMENTAL HEALTH AND SAFETY
Effective environmental, sustainability and chemical management is no longer simply about regulatory compliance. Increasingly these concerns are central components to companiesâ€™ strategic planning and management.
As a manufacturer of chemicals, all aspects of health and safety are of the utmost importance to enable continuity of supply to our valued customers. Our safety philosophy is not merely a statement but a role model for all of our employees to follow. To achieve this goal, a number of techniques are integrated into our manufacturing capabilities and processes.
Hazard and Operability Studies (HAZOP) HAZOPs identify possible causes of deviation, what the consequences might be and whether the correct safety feature can be installed or is present. The process is normally introduced at the plant design stage by a multi-disciplined team of professionals.
Fault Tree Analysis (FTA) FTA is primarily designed for product failure and trouble shooting and is characterized by each area of analysis creating its own chain or flow resulting in a fault being identified.
Risk Assessment All tasks follow a risk assessment procedure with the sole purpose of identifying hazards and ensuring control measures are in place to reduce the hazards to an acceptable level.
What If" All relevant procedures within our ISO 9002 accredited system carry a "what if" section which subsequently advises operatives as to the action required to eliminate any unexpected problems.
Control All Health & Safety aspects of the company business are audited to ensure compliance with legislative requirements, and to ensure employees are conforming to set procedures.