Skip to main content Skip to search Skip to main navigation

Sliding doors in cleanrooms - "no go" or "best practice"?

Shortened and edited excerpt from the GMP Compliance Adviser, Chapter 3.E "Cleanroom Construction Components"

5 min. reading time | by Harald Flechl / Doris Borchert (editorial editing)
Published in LOGFILE 35/2020

In cleanrooms, it is necessary to create a clear demarcation to adjacent, less clean areas. Since the beginning of clean room technology, airlocks have established themselves as an effective means of separating rooms.

The doors arranged one behind the other for access to the clean area must not be opened simultaneously in order to maintain the separation of the areas. This arrangement can still be seen as the state of the art in cleanroom technology.

Hinged doors, single or double-leaf with inactive and active leaves, striking plate, hinges and handle sets are the most frequently used doors in cleanrooms. But often undetected risks are concealed here:


Uncontrolled dead spaces

The retractable bottom seal (Figure 1) in hinged door leaves, which is often desired and installed because of the higher sealing tightness, does not meet the requirement for easy accessibility for cleaning. In the door leaf, an uncontrolled dead space results from the use of the seal, which is open at the end faces of the door leaf and allows cleaning only when the door leaf is removed.

A retractable bottom seal (Figure 1) in hinged door leaves is often requested and installed because of the higher sealing tightness, however it is not easy-to-clean. The seal results in an uncontrolled dead space in the door leaf, which is open at the end faces of the door and permits cleaning only when the door leaf is removed.

Figure 1 Integrated retractable bottom seal for hinged doors

A further risk is concealed in the locking mechanism of the doors. The fixtures including bolt, latch, door locks and the hinges are often overlooked as weak points. Most doors here have uncontrolled and hard to clean openings (striking plate open towards the entire door frame). Monoblock systems often offer the possibility of integrating door closers into the panel. These are not visible from the outside, but replacement should be possible.


Air turbulences

Manual opening of a hinged door creates a high air turbulence (depending on the opening speed of the door) which causes uncontrolled air exchange between adjacent rooms of different cleanroom classes. In order to enable smooth and steady closing and thus avoid the disadvantages mentioned above, cleanroom doors can be equipped with drives for automatic opening by sensors or by manual control units and also including door closers. The suitability of the drive for use in a clean room should be proven (e.g. suitability test by an independent institute). The safety requirements of the European harmonized product standard EN 13241 must be complied with. Thresholds or stop rails on the floor are not recommended.


Sliding doors as a solution to the problem?

In view of the risks and disadvantages mentioned above, the question inevitably arises as to whether sliding doors are a sensible and GMP-compliant alternative to the hinged doors normally used. With regard to sliding doors, Annex 1 of the EU GMP Guide recommends the following:

„To reduce accumulation of dust and to facilitate cleaning there should be no un-cleanable recesses and a minimum of projecting ledges, shelves, cupboard and equipment. Doors should be designed to avoid those uncleanable recesses; sliding doors may be undesirable for this reason.”

The word selection in the German translation of the text “sliding doors may be undesirable” was somewhat harsher than the original English intent, which in the past has led to a general distaste for sliding doors in GMP environments there, as it was interpreted that “sliding doors are not permitted”. Practical inspection experience has shown that in most cases sliding doors as well as high-speed rollup doors are accepted by the agencies for cleanroom applications.

When installing automatic sliding doors, it should be considered that the drives should be installed on the side with the lower cleanroom class (see view from side with higher cleanroom class in Figure 2).

Figure 2 Automated sliding door with status indicator, emergency stop and cleat (G+H Reinraumtechnik GmbH, D-67063 Ludwigshafen; www.guh-reinraumtechnik.de)

Analogously, the same recommendations apply for so-called high-speed doors (Figure 3), which roll up in the vertical direction to open and close.

Figure 3 High-speed door with electrical drive - clean room certification from Fraunhofer Institute (source: ASSA ABLOY Entrance Systems, www.assaabloyentrance.de)

Horizontal sliding doors and vertical rolling high-speed doors provide a number of decisive advantages in cleanrooms:

  • They have low space requirements.
  • As a result of their roll-down design, they provide effective seals on all four sides.
  • Undesirable strong turbulent air currents and pressure swings, which often occur when opening hinged doors, are avoided with this application.
  • High speed doors reduce the incursion of air and the potentially resulting cleanroom air contamination to a minimum. 

The following requirements are placed to achieve a GMP-compliant motorized or mechanical drive design:

  • The sliding door leaves are only attached at the upper side on a rolling carriage. Thresholds and floor rails are not recommended.
  • The complete drive unit and support rail should be enclosed according to dust protection standards, be sealed as well as possible and be mounted on the side of the wall with the lower cleanroom standard.
  • Technically, it is possible to connect the housing to the exhaust air pipe and to extract the particles generated therein (from abrasion) in a targeted manner (i.e. at "negative pressure" compared to the clean room).
  • The housing of the drive parts should be easy to open for inspection and cleaning purposes and also be easily accessible for cleaning.

The following safety aspects should be considered or installed

  • Safety specifications according to the European harmonised product standard EN 13241. The level of safety can be improved further by using a presence recognition system.
  • Emergency stop switch
  • Back-up battery or manual emergency opener
  • Regular safety checks according to agency, manufacturer and internal safety specifications

In view of the considerable advantages offered by sliding doors in clean rooms, this alternative should be considered more often in practice.

Do you know the legal requirements to be considered when selecting suitable components for pharmaceutical production? Are you interested in new technologies for planning? And would you like to get an overview of the state of the art for wall and ceiling systems, windows and doors as well as floor systems?

Then read the complete Chapter 3.E "Cleanroom Construction Components"in the GMP Compliance Adviser, the most comprehensive GMP online knowledge portal worldwide.


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

Harald Flechl
Harald Flechl

You may also be interested in the following articles:

Swissmedic Updates Guidance on GMP Compliance of Foreign Manufacturers

Swissmedic Updates Guidance on GMP Compliance of Foreign Manufacturers

Swissmedic has revised its guidance document “GMP compliance by foreign manufacturers”. The new Version 7.0 has been valid since 7 September 2026. In particular, it introduces new provisions for demonstrating the GMP compliance of manufacturers inspected by the US FDA. 
Read more
Swissmedic Updates Requirements for Cooperation with Pre-Wholesalers

Swissmedic Updates Requirements for Cooperation with Pre-Wholesalers

Swissmedic has revised its Technical Interpretation “Market release and distribution in cooperation with a pre-wholesaler”. The document addresses market release and distribution where a Marketing Authorisation Holder works with a pre-wholesaler (logistics and distribution service provider).
Read more
News: Europe

IPEC Updates Two Guides on Pharmaceutical Excipients

The IPEC Federation has updated two key guides on pharmaceutical excipients. The IPEC Composition Guide for Pharmaceutical Excipients (Version 3, 2026) describes an approach for manufacturers to establish excipient composition profiles. The revised version now covers biotechnology- and fermentation-derived excipients, provides further details on component types and physicochemical characterisation, and includes an example composition profile template.
Read more
Applying the FDA’s 7-Step Model for AI/ML Validation in GMP Environments: One Year Later

Applying the FDA’s 7-Step Model for AI/ML Validation in GMP Environments: One Year Later

Artificial intelligence is becoming increasingly important in GMP-regulated environments, presenting companies with new regulatory challenges. This article summarizes the latest regulatory developments, introduces a validation framework based on the FDA's seven-step model, and outlines initial practical experience with AI/ML validation.

Read more
Question of the Week | GMP-Verlag

What are the General Requirements for Standard Documents?

Here's the answer:
Read more
News: Europe

EDQM: Revised Guidance on Sister File Applications

The European Directorate for the Quality of Medicines & HealthCare (EDQM) has revised its Guidance on applications for “sister files” (PA/PH/CEP (09) 141). The revision is intended to support consistent application of the procedure and provide greater clarity on the classification and assessment of the corresponding CEP applications.
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.

delivery time appr. 2-5 workdays after receipt of payment
€1,368.00 net excl. VAT
GMP:KnowHow Pharma Logistics (GDP) | Named User Licence | 12M

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

Your knowledge portal for GDP-compliant pharmaceutical logistics.  It is important that you as a logistics service provider, but also as a client in the pharmaceutical industry, comply with regulatory requirements. The GMP:KnowHow knowledge portal guides you through the complex regulatory landscape of the pharmaceutical and logistical supply chain! The knowledge portal gives you an easy-to-understand overview of all the important topics. Interactive graphics help you navigate all 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 valuable research time.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? GMP:KnowHow Pharma Logistics (GDP) is a practical knowledge portal dedicated to Good Distribution Practice (GDP). 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, currently Director Quality at Fisher Clinical Services, previously served as Head of Quality Control and Responsible Person (GDP) for the Grieshaber Group. She is also a long-standing author and GDP expert at GMP-Verlag.

delivery time appr. 2-5 workdays after receipt of payment
€610.00 net excl. VAT
E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

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.The Author This e-learning course was developed with the collaboration of Dipl.-Ing. Andreas Nuhn (D & B Pharmadesign GmbH).

delivery time appr. 2-5 workdays after receipt of payment
€245.00 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.

delivery immediately after receipt of payment
€44.90 net excl. VAT