German
€0.00*

Parking disc

0 reviews

Average rating of 0 out of 5 stars

Leave a review!

Share your experiences with other customers.

Skip image gallery
This item is no longer available.
delivery time appr. 2-5 workdays after receipt of payment

€5.00

net excl. VAT

Product Information

Very sturdy parking disc, made of hard plastic, with 

  • ice scraper and rubber lip, 
  • 3 plastic coins for shopping carts, 
  • removable tire tread depth gauge on the back. 

The parking disc complies with the StVO (German Road Traffic Regulations). 

Please note that due to seasonal factors, delivery of this item may take approximately 2 to 3 weeks.

Do you Have any Questions?

Ansprechpartner beim GMP-Verlag

Talk to our customer advisors

Do you have any questions about our products and services? We are here to help.

Ihre persönliche Beratung

service@gmp-verlag.de +49 (0)7622 66686-70

Customer Reviews

0 reviews

Average rating of 0 out of 5 stars

Leave a review!

Share your experiences with other customers.

You may also be interested in the following products

Skip product gallery

l

Foldable bag

Foldable bag

The small package contains a voluminous bag with long handles. After use, simply fold the bag back up again. The cover is integrated into the bag. The package is light and small and even fits in your pocket. When unfolded, the bag measures approx. 40 x 40 cm. Environmentally friendly material: The rPET material is made from recycled PET, e.g., from soft drink bottles. Please note that due to seasonal factors, delivery of this item may take approximately 2 to 3 weeks. 

delivery time appr. 2-5 workdays after receipt of payment
€5.00 net excl. VAT
Details
Microfiber Cloth

Microfiber Cloth

Now you have the right GMP insight. Soft microfiber cloth printed with GMP-related motifs. Suitable for cleaning glasses, monitors, and mobile device displays. Easy to use: 24.5 cm x 24.5 cm in size. Please note that due to seasonal factors, delivery of this item may take approximately 2 to 3 weeks.

delivery time appr. 2-5 workdays after receipt of payment
€5.00 net excl. VAT
Details

Recommended Articles

Outsourced Activities in the GDP Environment Part II: Contractual Agreements
LOGFILE Feature

Outsourced Activities in the GDP Environment Part II: Contractual Agreements

When outsourcing GDP activities, there is a need for concrete delimitation of responsibilities between a client and a contractor. Read more about the goals and the contents of a quality agreement in the following excerpt from GMP:KnowHow Pharmalogistics (GDP).

Read more
Question of the Week | GMP-Verlag
Question of the Week

What are the Benefits and Limitations of Passive Temperature-Controlled Containers for Drug Transport?

Here's the answer:
Read more
FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines
News

FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines

The FDA has updated its recommendations on Acceptable Intake (AI) limits for nitrosamine impurities. Under certain conditions, the Agency now accepts a Less-Than-Lifetime (LTL) adjustment of AI limits for medicinal products that are not intended for lifetime use. This also represents an alignment with the LTL concept of ICH M7(R2).
Read more
Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates
News

Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates

As of 15 November 2026, active substances must be registered in the EMA's Substance Management Services (SMS) database before Swissmedic can include them in establishment licences and GMP certificates for active substance manufacturers. The new requirement results from modifications to the EudraGMDP database.
Read more
News: EMA
News

EMA: New Q&As for Biological Medicinal Products

The EMA has added a new section to its Q&As on biological medicinal products addressing medicinal products containing secretomes or extracellular vesicles (EVs) obtained from human or animal cells.
Read more
News: Europe
News

EU: Council Adopts the Pharmaceutical Package

On 28 September 2026, the Council of the European Union adopted the EU pharmaceutical package, marking another important step in the legislative process for the comprehensive reform of EU pharmaceutical legislation.
Read more
News: EMA
News

EMA: Report on First Bilateral Meeting with APIC Published

The EMA has published the highlights of its first bilateral meeting with the Active Pharmaceutical Ingredients Committee (APIC). Topics included GMP oversight of API manufacturers, the reuse of recovered solvents and nitrosamine risks.
Read more
Save Time and Money when Qualifying a Blister Packaging Line
LOGFILE Feature

Save Time and Money when Qualifying a Blister Packaging Line

Qualifying a blister packaging line is not only technically demanding, but also time-consuming and costly. Here you will find important tips on how to organise your qualification process in a cost-effective yet gmp-compliant manner.

Read more
Question of the Week | GMP-Verlag
Question of the Week

What is the Role of the Logistics Service Provider?

Here's the answer:
Read more
News: EMA
News

EMA: Latest Report on the International GMP Inspection Programme for API Manufacturers

EMA has published a new report on the International Active Pharmaceutical Ingredient Inspection Programme, covering the period 2017–2024. During this time, the number of participating authorities increased from ten to 13. Information was shared on 936 inspected sites and 1,684 inspections.
Read more
News: EMA
News

EMA Updates Procedure for Coordinating GMP Inspections

EMA has updated its procedure for coordinating GMP inspections for centrally authorised medicinal products. Version 3 has applied since 10 September 2026 and replaces Version 2. The document forms part of the Compilation of Union Procedures on Inspections and Exchange of Information (CoUP), which comprises the EU procedures and templates for GMP and GDP inspections.
Read more
Swissmedic Updates Guidance on GMP Compliance of Foreign Manufacturers
News

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
Previous
Next
This website uses cookies to ensure the best experience possible. More information...