Skip to main content Skip to search Skip to main navigation

12 FREQUENTLY ASKED QUESTIONS on SOPs

Excerpt from the DHI/PDA Book SOPs Clear and Simple: For Healthcare Manufacturers

7 min. reading time | by Brian Matye, Jeanne Moldenhauer, Susan Schniepp
Published in LOGFILE 19/2020

Question: How often should I review my SOPs?

Answer: SOPs should be reviewed at least every two years. If an SOP is revised in between the two-year window, it should be reviewed thoroughly at the time of a revision. If the proposed revision affects related SOPs, they should also be reviewed for impact before the SOP revision is made affective.


Question: How many SOPs should I have in my system?

Answer: There is no set rule or formula regarding the number of SOPs needed for a functioning system. The number of SOPs needed depends on the activities the company is performing. We recommend writing SOPs that reflect your operations and avoid having SOPs in your system for operations you do not perform.


Question: What format do you recommend for SOPs?

Answer: There is no one correct format for SOPs. The format you chose will depend on the operation you are defining and the  experience and makeup of your workforce. Acceptable formats for SOPs include using play script, general paragraph form, flow charts, pictorial or any combination to communicate the SOP operation to the workforce. Whatever style you decide to use be sure that your SOP format includes the following recommended elements:

Unique identifying number and title
Effective date
Purpose and scope
Roles and responsibilities
Change history
Official signatures
Step-by-step instructions

 


Question: What do I do when I obsolete an SOP?

Answer: You should only obsolete an SOP if your company is no longer performing the activity described by the SOP. The SOP should be obsoleted using the change control system. It is critical that you review SOPs related to the one you are obsoleting and determine if they need revision as a result of the obsoleted SOP. In addition, any forms associated with the obsoleted SOP should be collected and destroyed. The obsoleted SOP and associated forms should remain on file in case they need to be referred to but they should clearly be stamped as being obsoleted.


Question: How much time should I allow for training on SOPs?

Answer: There is no set time regarding the amount of time allowed for training on SOPs. The amount of time needed to train on an SOP depends on your operation. Companies with multiple sites affected by the SOP may need additional time to train than a smaller company with just one site. We recommend, as a general rule, that you allow two weeks to train on an SOP.


Question: What is the difference between a release date and an effective or official date?

Answer: The release date for an SOP indicates that the necessary revisions have been approved and the SOP is ready and available for training. Once the training is complete and documented, the SOP can be made official and used by the employees performing the described operation. We recommend, as a general rule, that you allow two weeks to train on an SOP before you make it official.


Question: Should a company use the same date format whatever it decides or can a variety of formats be used provided the date is clear and legible?

Answer: Dictating one date format versus another can create unnecessary and irrelevant deviations. The requirements for the date are that it should be legible and readable. Acceptable date formats include:

mm-dd-yy, where the month, day and year are numerical separated by hyphens.
mm/dd/yy, where the month, day and year are numerical separated by slashes.
30 Aug15 or 30 Aug 2015, where the day and year are numeric and the month is alphabetic.

Whether you decide to specify a date format or not, remember that the critical elements for a date if legibility and readability.


Question: When pictorials are used, is it recommended to reference the SOP number?

Answer: Yes. This will make it much easier to track the documents for necessary revisions.


Question: Are electronic signatures acceptable on SOPs?

Answer: Yes, electronic signatures are acceptable on SOPs. We recommend that if you have electronic signature capabilities be sure you comply to 21 CFR 11 and can provide an audit trail upon request. In addition, we recommend that individuals who have the authority to approve SOPs electronically have a unique account and password to avoid any data integrity issues.


Question: Can you have two different expiry dates? For example, SOPs for instruments reviewed every four years and SOPs regarding quality systems (OOS, OOT, change control, audits) every two years.

Answer: Yes, you can have two different review periods for various SOPs in the system. You should document your rationale for why you have chosen these time frames for review. However, whether you review your SOPs on a two-year or four-year cycle, SOPs revised in between the defined cycle should be reviewed thoroughly at the time of a revision. If the proposed revision affects related SOPs, they should also be reviewed for impact before the SOP revision is made affective, regardless of what cycle period they are on.


Question: If an SOP gives step-by-step instructions then what is a “workinstruction” and when would it be necessary?

Answer: There really is no need for work instructions if you write your SOPs in a clear and concise manner.


Question: Is there an expectation that the change history be contained within the SOP?

Answer: Common industry practice is to include the change history of the SOP within the document but there is no requirement that you must include it in the document. If you chose not to include the change history in the document be sure you capture it in a controlled system that is available for answering questions during an inspection or audit.



Do you have any questions or suggestions? Please contact us at: redaktion@gmp-verlag.de

You may also be interested in the following articles:

How is a QRM process initiated?

How is a QRM process initiated?

You can view the answer here:
Read more
FDA: Updated Pre-RFD Guidance for Combination Products

FDA: Updated Pre-RFD Guidance for Combination Products

The U.S. FDA has released an updated final guidance on preparing a Pre-Request for Designation (Pre-RFD), replacing the previous 2018 version. The revised document provides new recommendations for interacting with the Office of Combination Products (OCP) and clarifies expectations for Pre-RFD submissions.
Read more
EDQM: 9 Virtual Training Modules on Ph. Eur. and CEPs

EDQM: 9 Virtual Training Modules on Ph. Eur. and CEPs

The EDQM has introduced a modular training programme covering chemically defined active substances and medicinal products. It will take place between 1 and 12 December 2025.
Read more
Previous
Next

Related Products

Skip product gallery
GMP Compliance Adviser | Named User Licence | 12M

GMP Compliance Adviser | Named User Licence | 12M

The GMP Compliance Adviser is an online publication that covers all aspects of Good Manufacturing Practice (GMP) in one source.In the GMP Compliance Adviser you’ll find: GMP in Practice This part contains 21 chapters with GMP expert knowledge to base your decisions upon. It provides practical assistance with checklists, templates and SOP examples. It is written by more than 80 authors with hands-on experience directly linked to the industry. The individual chapters describe the different aspects of GMP in clear language. Technical, organizational and procedural aspects are covered.More than 700 checklists, templates and examples of standard operation procedures taken directly out of practice help you in understanding the GMP requirements.GMP RegulationsThese chapters cover the most important GMP regulations from Europe and the United States (CFR and FDA), but also PIC/S, ICH, WHO and many more.  Sample Documents In addition, the GMP Compliance Adviser contains many sample documents and practical examples that you can use.

Ready for dispatch, Delivery time appr. 2-5 workdays (2-3 weeks for christmas goodies)
€1,335.00 net excl. VAT
GMP:KnowHow Pharma Logistics (GDP) | Named User License | 12M

GMP:KnowHow Pharma Logistics (GDP) | Named User License | 12M

Your knowledge base about GDP-compliant handling of your pharmaceutical logistics. It is important that you as a logistics service provider, but also as a client in the pharmaceutical industry, adhere precisely to the regulatory requirements. The GMP:KnowHow knowledge portal guides you through the regulatory jungle of the pharmaceutical and logistical supply chain! The knowledge portal gives you an easy-to-understand overview of all the important topics. Using graphics, you can easily navigate through all the areas covered by the EU GDP Guidelines (2013/C 343/01). You also have the relevant passages of the regulations directly at hand for each topic. This allows you to compare the requirements directly and saves you a lot of time on time-consuming searches and research!One thing is certain: the knowledge portal answers your questions about the supply chain of medicinal products, active pharmaceutical ingredients and medical devices. You don't have to be an expert. Yet.You will find answers to your questions in the GMP:KnowHow Pharma Logistics (GDP). Where does GDP begin, where does GMP end? What does GDP-compliant mean? When do I also have to take GMP requirements into account? What permits do I need for certain activities? What requirements do I have to fulfil? What is the current legal basis? How am I covered? What authorizations do I have for my work, e.g. from my employer? Who is responsible — the client or the contractor? And many more What is the difference to the GMP Compliance Adviser? The GMP:KnowHow Pharma Logistics (GDP) is your guideline for Good Distribution Practice. It is a product that is independent of the GMP Compliance Adviser and concentrates on content that is essential for carriers of medicinal products, active pharmaceutical ingredients and medical devices as well as for logistics clients. The focus is on practical knowledge and how to apply it in your daily business. If necessary, the relevant regulations can be called up immediately alongside the practical knowledge, and you can see the relevant paragraphs at a glance. In addition, sample documents are available to help you make immediate progress. AuthorSimone Ferrante – now Director Quality at Fisher Clinical Services – was previously Head of Quality Control and Responsible Person according to GDP (VP) for the entire Grieshaber Group. She is also a long-standing author and GDP expert at GMP-Verlag.

Ready for dispatch, Delivery time appr. 2-5 workdays (2-3 weeks for christmas goodies)
€610.00 net excl. VAT
E-Learning GMP:READY | GMP for Engineers Online Course

E-Learning GMP:READY | GMP for Engineers Online Course

Why are GMP rules important for technicians and engineers? Technicians and engineers play a key role in ensuring compliance with Good Manufacturing Practice (GMP) standards. They are involved in critical activities such as: planning and construction of ventilation systems, maintenance of water treatment plants, calibration of measuring sensors. Therefore, they are jointly responsible for the quality of medicines and must ensure that their work complies with GMP standards.Your advantages: Fast familiarization with GMP topics in approx. 2 hours, time- and location-independent online training, printable personal certificate, 12-month access for initial and follow-up training, automatic updates in case of legal changes, content compliant with Article 7(4) of Directive 2003/94/EC.

Ready for dispatch, Delivery time appr. 2-5 workdays (2-3 weeks for christmas goodies)
€240.00 net excl. VAT
GMP Fundamentals | A Step-by-Step Guide

GMP Fundamentals | A Step-by-Step Guide

This handbook is a practical and easy to read guideline, giving you a quick and comprehensive overview of the complex world of Good Manufacturing Practice (GMP) without the need of previously acquired knowledge. Some topics are: GMP: Purpose and basic pharmaceutical terms Laws, licenses and inspections Personnel: Responsibility and hygiene Standard Operating Procedures (SOP) and documentation Design of rooms and facilities Processing and packaging Quality control and market release Suppliers, storage and logistics (Good Distribution Practice = GDP) Alphabetical index and abbreviations Using practical examples and comparisons to every-day life will help to easy understand GMP regulations.GMP Fundamentals is a helpful guide which facilitates the entry into the GMP world and teaches the necessary basics.

Ready for dispatch, delivery immediately after receipt of payment
€44.90 net excl. VAT