Testing & Inspection
TÜV Austria India > Solution > Industry > Product Certification & CE Marking Solution: Product Certification & CE Marking Testing & Inspection Solution: Product Certification & CE Marking TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office) TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office) TÜV AUSTRIA \| India Office No. 302, Plot no. 95, Renuka Complex, Friends Colony, Katol Road 440013 Nagpur/Maharashtra India +917124033988 Send email Office No. 302, Plot no. 95, Renuka Complex, Friends Colony, Katol Road 440013 Nagpur/Maharashtra India TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office) TÜV AUSTRIA is a Member in Good Standing of TIC Council \| TÜV (R) Product Certification & CE Marking: Conformity Assessment for EU Market Access "Achieve CE marking with structured product certification support: directive mapping, harmonised standards, risk assessment, testing, technical documentation and EU Declaration of Conformity." Product Certification & CE Marking: Conformity Assessment for EU Market Access CE marking is not a logo exercise; instead, CE marking follows a structured compliance process that demonstrates conformity with applicable EU requirements before a product enters the market. Therefore, we support manufacturers from the first compliance decision to final file readiness: we identify the relevant EU legislation, map suitable harmonised standards, plan testing and risk assessment, and build a technical file that supports the EU Declaration of Conformity and the CE marking. Moreover, we keep the documentation practical and audit-ready so you can respond quickly if market surveillance authorities request evidence. As a result, you gain clarity, speed, and better control over product compliance. Key Directives & Regulations Products can fall under more than one EU legal act, so first we map the product’s function, intended use, and risk profile. Then we align your design, testing, and documentation to the correct requirements. For example, a product may trigger both EMC and safety requirements depending on the configuration. Common examples include: Cableway Installations — (EU) 2016/424 ATEX (Explosive Atmospheres) — 2014/34/EU Electromagnetic Compatibility (EMC) — 2014/30/EU Construction Products — (EU) No 305/2011 Lifts & Safety Components — 2014/33/EU Personal Protective Equipment (PPE) — (EU) 2016/425 Machinery — 2006/42/EC Transportable Pressure Equipment — 2010/35/EU Radio Equipment — 2014/53/EU Pressure Equipment — 2014/68/EU Simple Pressure Vessels — 2014/29/EU Hot-water Boilers — 92/42/EEC Noise Emissions (Outdoor Equipment) — 2000/14/EC EU Fertilising Products — 2019/1009/EU What we do during product certification We translate legal requirements into clear actions. Additionally, we help you organize evidence, so you avoid rework later. Typical support includes: Requirement mapping: we confirm which directives/regulations apply and why Standards strategy: we select standards that best demonstrate compliance Documentation planning: we define what you must create, update, and retain Conformity route selection: we determine whether you can self-assess or you need third-party involvement, depending on scope Procedure to obtain CE marking (end-to-end) We follow a step-by-step route that keeps compliance controlled and traceable. Consequently, teams can move faster without missing mandatory steps. Identify applicable EU directives/regulations (products can be multi-directive) Apply harmonised standards to build a strong compliance route; use is typically voluntary but supports “presumption of conformity” where relevant. Perform risk assessment and required testing to demonstrate essential requirements are met. Compile technical documentation (design, manufacture, operation, risk analysis, test evidence, instructions, etc.). Carry out conformity assessment (may involve a Notified Body depending on product/module). Issue the EU Declaration of Conformity supported by the technical file. Affix the CE marking and maintain the file for market surveillance requests. Value delivered We focus on outcomes that reduce uncertainty and accelerate market access. Moreover, we keep the compliance package easy to maintain. End-to-end support from identification to declaration and file readiness Quicker EU market access through a clean, standards-led conformity route Reduced risk of rework by aligning testing, risk controls, and documents from the start Support with third-party involvement when mandatory, including typical Notified Body roles (review, testing, certification modules). More Tags: Automotive Technical & Industrial inspection Industry Machinery Third party Inspection Related solutions from the same sector: Machinery Vendor Assessment Industry Show more Supplier Quality Services Industry Show more NDT Services (Non-Destructive Testing) Industry Show more Plant Safety: What-If & SWIFT Industry Show more All Solutions Discover more sectors: Industry Automotive Municipalities Communications Technology Sustainability Trade & Commerce Agriculture Tourism Foodstuffs Transport & Traffic Certification Construction & Real Estate Electronics Leisure & Entertainment Health & Medicine Energy TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office) +917124033988 \| mailto:info.india@tuvaustria.com
TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office) +917124033988 \| mailto:info.india@tuvaustria.com

TÜV Austria India > Solution > Industry > Product Certification & CE Marking

Solution: Product Certification & CE Marking

Testing & Inspection

TÜV AUSTRIA INDIA PVT. LTD. – Nagpur/Maharashtra (Corporate Office)

TÜV AUSTRIA | India

Office No. 302, Plot no. 95, Renuka Complex, Friends Colony, Katol Road 440013 Nagpur/Maharashtra India

+917124033988

Send email

TÜV AUSTRIA is a Member in Good Standing of TIC Council | TÜV (R)

Product Certification & CE Marking: Conformity Assessment for EU Market Access

"Achieve CE marking with structured product certification support: directive mapping, harmonised standards, risk assessment, testing, technical documentation and EU Declaration of Conformity."

Product Certification & CE Marking: Conformity Assessment for EU Market Access

CE marking is not a logo exercise; instead, CE marking follows a structured compliance process that demonstrates conformity with applicable EU requirements before a product enters the market. Therefore, we support manufacturers from the first compliance decision to final file readiness: we identify the relevant EU legislation, map suitable harmonised standards, plan testing and risk assessment, and build a technical file that supports the EU Declaration of Conformity and the CE marking. Moreover, we keep the documentation practical and audit-ready so you can respond quickly if market surveillance authorities request evidence. As a result, you gain clarity, speed, and better control over product compliance.

Key Directives & Regulations

Products can fall under more than one EU legal act, so first we map the product’s function, intended use, and risk profile. Then we align your design, testing, and documentation to the correct requirements. For example, a product may trigger both EMC and safety requirements depending on the configuration.

Common examples include:

Cableway Installations — (EU) 2016/424
ATEX (Explosive Atmospheres) — 2014/34/EU
Electromagnetic Compatibility (EMC) — 2014/30/EU
Construction Products — (EU) No 305/2011
Lifts & Safety Components — 2014/33/EU
Personal Protective Equipment (PPE) — (EU) 2016/425
Machinery — 2006/42/EC
Transportable Pressure Equipment — 2010/35/EU
Radio Equipment — 2014/53/EU
Pressure Equipment — 2014/68/EU
Simple Pressure Vessels — 2014/29/EU
Hot-water Boilers — 92/42/EEC
Noise Emissions (Outdoor Equipment) — 2000/14/EC
EU Fertilising Products — 2019/1009/EU

What we do during product certification

We translate legal requirements into clear actions. Additionally, we help you organize evidence, so you avoid rework later.

Typical support includes:

Requirement mapping: we confirm which directives/regulations apply and why
Standards strategy: we select standards that best demonstrate compliance
Documentation planning: we define what you must create, update, and retain
Conformity route selection: we determine whether you can self-assess or you need third-party involvement, depending on scope

Procedure to obtain CE marking (end-to-end)

We follow a step-by-step route that keeps compliance controlled and traceable. Consequently, teams can move faster without missing mandatory steps.

Identify applicable EU directives/regulations (products can be multi-directive)
Apply harmonised standards to build a strong compliance route; use is typically voluntary but supports “presumption of conformity” where relevant.
Perform risk assessment and required testing to demonstrate essential requirements are met.
Compile technical documentation (design, manufacture, operation, risk analysis, test evidence, instructions, etc.).
Carry out conformity assessment (may involve a Notified Body depending on product/module).
Issue the EU Declaration of Conformity supported by the technical file.
Affix the CE marking and maintain the file for market surveillance requests.

Value delivered

We focus on outcomes that reduce uncertainty and accelerate market access. Moreover, we keep the compliance package easy to maintain.

End-to-end support from identification to declaration and file readiness
Quicker EU market access through a clean, standards-led conformity route
Reduced risk of rework by aligning testing, risk controls, and documents from the start
Support with third-party involvement when mandatory, including typical Notified Body roles (review, testing, certification modules).