R2 Responsible Care SERI Certification

SERI R2 CERTIFICATION DELHI, MUMBAI, HYDERABAD

TAJ Computers with its collection centre in Bangalore and processing centre in New Delhi has kick started the R2 Responsible care certification process. Lead by our Senior consultant, the gap analysis based on the standard have been conducted and the documentation process has been kick started.

R2 Responsible care 2013 published by SERI USA is a standard based on recycling electronic goods except for White goods. Right from collection till final disposal, the entire life cycle assessment is carried out and documents based on the standard are prepared. Implementation time frame will take any where between 6 to 12 months depending upon the maturity of the systems implemented.

The provisions of the R2 standard will have to be strictly adhered to achieve the certification from SERI approved certification body.

Looking for a SERI approved R2 Consultant, R2 Certified Recycler in DELHI, MUMBAI, HYDERABAD, CHENNAI or any part of the India, Singapore, Malaysia, Qatar, Oman, UAE, Philippines, Hongkong, Japan, Korea, Vietnam, Taiwan, Cambodia…Just drop an email to shakti@gqsindia.com or call or WhatsApp + 91 9741501910

ISO 50001:2011 Certification Goa

ISO 50001 Training, ISO 50001 Consulting Goa, ISO 50001 Consultancy Goa

Right from conducting Energy audit, Identification of the Significant Energy Use, Documenting over 120 Operational control criteria for various equipments, Identification of Design of new equipments which would reduce power consumption by 45%, Introducing Green Procurement, Identification & Installation of Sub-metering, Calibration of instruments of Operational criteria, Checking Efficiency of HVAC, Delta T of Cooling towers and a whole lot of milestones to reach this stage of Internal auditing for ISO 50001 Energy management at this plant in Goa where the power consumption is over few thousand Megawatt per day !!

Should your company be interested in ISO 50001 Training, ISO 50001 Consulting Goa, ISO 50001 Consultancy Goa, ISO 50001 Certification, call us on 9845313910 or drop an email to SHAKTI@GQSINDIA.COM

ISO 9001:2015 Risk Based thinking training

ISO 31000 Risk based thinking

ISO 31000 – Risk management standards were published keeping in mind that the clause on Preventive action will be sooner or later be obsolete.

Since 2012 all standards being published be it ISO 22301, ISO 27001, ISO 9001, ISO 14001, ISO 50001-2019, ISO 45001 (yet to be published) Addressing risks has become an important part of all management system and is mandatory for organisations to carry out a Risk assessment using any kind of tool such as FMEA, PESTLE, SWOT.

The training at HYCOM Engineers on ISO 31000 and Risk based thinking was carried out to all the team members. The Workshops have helped the team to understand the methodology to conduct the RA and also arrive at a decision method to reduce or eliminate the risks.

The following 4T Rule can be applied to reduce or terminate the risks

1. TERMINATE
2. TREAT
3. TRANSFER
4. TOLERATE

Interested to learn more about Risk assessment or Risk based thinking call 9845313910 or 9845078743 or drop an email to SHAKTI@GQSINDIA.COM

FSSC 22000 Version 4.1 Certification Consultants Bangalore Goa Mangalore

FSSC 22000 Version 4.1 Certificate, FSSC 22000 Version 4.1 Consultant

FSSC 22000 Version 4.1 Certification, FSSC 22000 Version 4.1 Consultant

Vijayanagara Sugar Gangapura completes its FSSC 22000 Version 4.1 Consultancy and documentation project. The entire team of the plant was involved in preparing the TACCP, VACCP for the product right from the Cane until the sugar is transported to the customer.

The changes from FSSC 22000 Version 3.1 to Version 4.1 were explained to the team and the team appreciated the effort by GQS to impart the training to the entire FSMS Team. The FSMS Team Leader applauded the smart way of preparing the TACCP and VACCP assessment workshop. The workshop was very interactive and was tailor made to suit the sugar industry.

Should you be interested in FSSC 22000 Version 4.1 certification or consultancy drop an email or call us on 9845313910 or 9845078743.

HALAL ISO 22000 FSSC 22000 V4.1 Certification Fruit Jam Processing

HALAL ISO 22000 FSSC 22000 V4.1

HALAL ISO 22000 FSSC 22000 V4.1

Call 9845313910 or 9845078743 to know more details

How to prepare VACCP, TACCP for FSSC 22000 V4.1

TACCP, VACCP

How do you carry out assessment of TACCP, VACCP and ready your organization for FSSC 22000 V4.1

While HACCP helps you identify the scientific reasons to reduce Food safety incidents, TACCP and VACCP have different intent.

TACCP – Threat Assessment Critical Control Point have been incorporated in many FSMS standards such as FSSC 22000 Version 4.1, BRC, SQF and many more in the form of Food defence mechanism.

Threats foreseen or unforeseen from various sources such as Disgruntled individuals, Extremists, Opportunist, Cyber criminal, Extortionist are assessed and prioritised. This is also referred to Behaviour Motivated Adulteration.

Top Priority threats are considered as Critical control point and treated or terminated using Protective controls. These controls have to be reviewed atleast annually or as and when an incident occurs. Guidelines such as PAS 96 can be used as a reference and basis to assess the threats and prioritise them.

VACCP – Vulnerability Assessment Critical control point have also been incorporated in BRC, FSSC 22000 V4.1.

Organisations who are certified to FSSC 22000 V3.1 and upgrading to FSSC 22000 V4.1 should ensure that a separate Assessment is carried out emphasising on Economically Motivated Adulteration EMA. All such risks are assessed and prioritised to ensure that appropriate Protective controls are established, followed with pre determined review mechanism.

Still have doubts in TACCP, VACPP, FSSC 22000 V4.1 do call us on 98453 13910, 98450 78743 or drop an email to SHAKTI@GQSINDIA.COM

How to to achieve BA 9000 Body Armour Management System  Certification

How to to achieve BA 9000 Body Armour Management System  Certification

Step 1 – Buy the BA 9000 Standard

Step 2 – Hire GQS an approved consultant

Step 3 – Prepare Manual

Step 4 – Prepare Procedures and forms

Step 5 – Conduct Risk assessment.

Step 6 – Conduct Internal auditor training

Step 7 – Conduct Internal audit and Management review meeting

Step 8 – Identify accredited certification body

Step 9 – Certifying body conducts Stage 1 audit

Step 10 – Certifying body conducts Stage 2 audit

Contact SHAKTI@GQSINDIA.COM

Call 98450 78743 or 9845313910 to know further details about BA 9000 Body Armour Certification.

How to get ISO 45001-2018 Certification

How to to get ISO 45001:2018 Certification

Step 1 – Buy the ISO 45001:2018 Standard once the final standard is published

Step 2 – Hire an approved consultant.

Step 3 – Prepare ISO 45001:2018 Manual

Step 4 – Prepare Procedures and forms on ISO 45001:2018

Step 5 – Conduct Risk assessment ISO 45001:2018

Step 6 – Conduct Internal auditor training on ISO 45001:2018

Step 7 – Conduct Internal audit and Management review meeting

Step 8 – Identify accredited certification body

Step 9 – Certifying body conducts ISO 45001:2018 Stage 1 audit

Step 10 – Certifying body conducts ISO 45001:2018 Stage 2 audit

Contact SHAKTI@GQSINDIA.COM

Call 98450 78743 or 9845313910 to know further details about ISO 45001:2018 Certification.

CTDI Regenersis is now R2 Responsible recycling SERI Certified ANAB Accredited

R2 Responsible Recycling SERI Certificate SERI ANAB

CTDI Regenersis is now R2 Responsible recycling SERI Certified ANAB Accredited

GQS is proud to announce that our client is now certified to the world renowned R2 Responsible recycling certificate provided by SERI approved and ANAB accredited certification body.

The entire exercise took over 5 months for thorough R2  implementation, R2 in-depth training to core team, R2 Internal auditing, Management review based on R2 Requirements, R2 SERI Licensing and subsequent R2 Certification audit. The certificate is valid for 3 years and during which there would also be a visit by SERI to check compliance levels at the factory.

Should you be interested to be a part of the Sustainable recycling and wish to be R2 Responsible recycling certified do call us on +91 9845313910 or drop an email to SHAKTI@GQSINDIA.COM

Services offered in Bangalore, Singapore, Thailand, UAE, Kuwait, Qatar, Oman, Philippines, Malaysia – Penang, Kuala lumpur, Ipoh; Indonesia – Jakarta, Batam Islands

EFFCI Certification support, EFFCI Consultancy, EXCIPACT Certification

EFFCI – Coverage in 2 Days

1. Introduction to EFFCI, the European Federation for Cosmetic Ingredients, the organization and functioning
2. Regulatory context for cosmetic ingredients in the EU and other parts of the world. International cosmetic legal and regulatory data base.
3. European cosmetic directive and EFFCI – Position of European Medicines Agency related to cosmetic ingredients
4. What are position papers published by EFFCI from time to time, their applicability, importance with examples
5. Importance of GMP’s in cosmetic ingredients and possible impact on consumer health
6. Risk analysis related to use of cosmetic ingredients in cosmetic products
7. Differences between ISO 22716 and EFFCI
8. Understanding the EFFCI standard in detail with interpretations
9. Process of certification to EFFCI.
10. What to expect during a Cosmetic GMP audit for ingredients? How to address the expectations of auditors?
11. Case studies to test the understanding of participants – How cosmetic GMP’s and applied in manufacturing context?
12. Customer specific requirements shall be included after understanding the context of training and objectives.

IPEC – EXCIPACT – Coverage in 3 Days

1. Introduction to IPAC-EXCIPACT, the standard for pharmaceutical excipients, the organization and functioning, its mission, vision and values.
2. Benefits of EXCIPACT scheme
3. Regulatory context for Pharma excipients various regions across the world. International legal and regulatory data base.
4. WHO-GMP requirements for pharmaceutical excipients
5. Importance of GMP’s in Pharmaceutical excipient industry and possible impact on consumer health
6. Risk analysis related to use of pharmaceutical excipients
7. The ISO 9001:2008 standard, basis of Excipact standard – How to adopt QMS in a excipient industry?
8. GMP and GDP standards suitable for 3rd party auditing
9. Definition of auditor competency for the delivery of the scheme
10. Certification scheme rules for 3rd party audit organizations
11. Publication, communication and on-going maintenance of the schemes, standards and guides developed.
12. Understanding the EXCIPACT standard in detail with interpretations
13. Process of certification to EXCIPACT.
14. What to expect during a GMP audit for Excipients? How to address the expectations of auditors?
15. Case studies to test the understanding of participants – How GMP’s are applied in manufacturing context?
16. Customer specific requirements shall be included after understanding the context of training and objectives.