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SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

ComplianceOnline

Thursday, February 9, 2017 at 8:30 AM - Friday, February 10, 2017 at 3:30 PM (MST)

SOPs for FDA-Regulated Industry: Best Practices to...

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration (Early bird price)
For Registrations after January 20, 2017 - $1899
Feb 9, 2017 $1,499.00 $0.00
Seminar One Registration Feb 9, 2017 $1,899.00 $0.00

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Event Details

Course Description:

One of the best ways to ensure that an organization meets its regulatory obligations is to follow SOPs. SOPs are standardized procedures and processes prepared with enough detail to ensure that tasks are performed consistently each time they are done. SOPs are also required to be in compliance with regulations and guidelines internationally, across all regulated functions. Lack of SOPs and not following SOPs are often cited in regulatory inspections as deficiencies that must be corrected. Poorly prepared SOPs or poor compliance with existing SOPs can compromise a drug development program, an effective quality system, and may result in product recalls.

This workshop will explore what SOPs are, what they are used for, when they are required, how to write them effectively for compliance and for implementation within the organization, and how to ensure effective communication and training of procedures within the SOPs.

Learning Objectives:

  • Regulatory requirements for SOPs
  • Legal requirements for SOP creation and maintenance
  • Types of SOPs
  • Formats and essential components of SOPs
  • How to effectively write an SOP to ensure compliance
  • SOP training and implementation
  • Deviations from and changes to SOPs

 

Who Will Benefit:

This workshop will be beneficial for individuals supporting clinical trials, manufacturing, distribution, marketing, regulatory affairs, compliance, quality control, and quality assurance:

  • Directors
  • Managers
  • Supervisors
  • Auditors
  • Regulatory operations
  • Clinical investigators, site management and contracting personnel
  • Clinical operations
  • Project managers
  • Data management
  • Medical writers
  • Compliance officers
  • Anyone required to create SOPs for their job function in a regulated industry

 

For Registrationhttp://www.complianceonline.com/sops-for-fda-regulated-industry-seminar-training-80412SEM-prdsm?channel=eventbrite          

 

Note: Use coupon code < NB5SQH8N > and get 10% off on registration.

Have questions about SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations? Contact ComplianceOnline

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When & Where


Scottsdale

Scottsdale, AZ

Thursday, February 9, 2017 at 8:30 AM - Friday, February 10, 2017 at 3:30 PM (MST)


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Organizer

ComplianceOnline

Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.

Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.

Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations
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