Pharmaceutical Quality; GxP Training, Consulting and Auditing Services
Offering You Practical Solutions With Outstanding Results
NSF International has expanded its range of services, bringing additional pharma and biotech expertise to you directly, when you need it.
Our new and expanded remote and virtual auditing and consultancy services can provide you with the tools you need to stay agile and proactive during this time. With rapid access to our credible and seasoned experts, we can help you to develop timely responses to the challenges that lay ahead. Contact our team today – we’re here to help.
About NSF: Global Experts for Pharmaceutical Consulting, Auditing and Training
Our Remote Services
REMOTE AND VIRTUAL GMP AUDITS
NSF’s four-step process for remote GMP auditing can help you to unlock supply chains and meet cGMP needs. Using our network of international GMP experts, e-rooms and videoconferencing, NSF can offer a hybrid approach to auditing that is both insightful and timely.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
Watch the latest webinar 'An Update on Remote and Virtual GMP Audits’ >>
INSTRUCTOR-LED VIRTUAL TRAINING AND eLEARNING
NSF’s virtual training courses are delivered via a combination of live instructor-led virtual classrooms and independent pre- and post-course activities. Our expert coaches will be on hand throughout to guide you through the interactive sessions.
NSF’s self-paced eLearning can be completed at a time and place to suit you. They include targeted and highly focused ‘how to’ sessions on common industry themes as well as essential introductions and overviews to those new to the industry.
All training can be tailored to suit your organizational needs, do not hesitate to get in touch to discuss your requirements.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
REMOTE GxP CONSULTANCY
NSF’s remote consultancy service can provide you with quick, accurate and practical guidance on the challenges that lay ahead. Our four expanding services include:
- Live consultancy
- 1-1 management & technical coaching
- Remote review and authorship of local policies and procedures
- Remote support to your pharma quality system
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
New NSF Journal: Time to Rethink
Featured articles:
- Rethinking leadership, supply chains, vaccine development, and managing business in an uncertain world
- Streamlining operations in a COVID-19 environment
- Meeting FDA submission requirements when developing and implementing changes to risk evaluation and mitigation strategies (REMS)
- A detailed regulatory update section, including a review of the U.S. regulatory preparedness in facing the COVID-19 pandemic.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
Remediation Case Study
GMP remediation projects are rarely just about upgrading SOPs and retraining staff. John Johnson shares how the best firms use remediation projects proactively to alter the mind-set for quality and reduce ongoing costs to the business.
Get In Touch
Have a question or want more information about our services?
Contact our team at pharmamail@nsf.org or visit www.nsfpharma.org.
SIGN UP FOR YOUR COMPLIMENTARY JOURNAL AND MONTHLY E-JOURNAL
REMOTE AND VIRTUAL GMP AUDITS
NSF’s four-step process for remote GMP auditing can help you to unlock supply chains and meet cGMP needs. Using our network of international GMP experts, e-rooms and videoconferencing, NSF can offer a hybrid approach to auditing that is both insightful and timely.
Watch the latest webinar 'An Update on Remote and Virtual GMP Audits’ >>
INSTRUCTOR-LED VIRTUAL TRAINING AND eLEARNING
NSF’s virtual training courses are delivered via a combination of live instructor-led virtual classrooms and independent pre- and post-course activities. Our expert coaches will be on hand throughout to guide you through the interactive sessions.
NSF’s self-paced eLearning can be completed at a time and place to suit you. They include targeted and highly focused ‘how to’ sessions on common industry themes as well as essential introductions and overviews to those new to the industry.
All training can be tailored to suit your organizational needs, do not hesitate to get in touch to discuss your requirements.
REMOTE GxP CONSULTANCY
NSF’s remote consultancy service can provide you with quick, accurate and practical guidance on the challenges that lay ahead. Our four expanding services include:
- Live consultancy
- 1-1 management & technical coaching
- Remote review and authorship of local policies and procedures
- Remote support to your pharma quality system
NEW NSF JOURNAL: TIME TO RETHINK
Featured articles:
- Rethinking leadership, supply chains, vaccine development, and managing business in an uncertain world
- Streamlining operations in a COVID-19 environment
- Meeting FDA submission requirements when developing and implementing changes to risk evaluation and mitigation strategies (REMS)
- A detailed regulatory update section, including a review of the U.S. regulatory preparedness in facing the COVID-19 pandemic.