deck_19247894

Question 1

How many sections are in an SDS?

Answer 1

16 sections

Question 2

List all SDS sections in order.

Answer 2

1) Identification 2) Hazards identification 3) Composition/information on ingredients 4) First-aid measures 5) Firefighting measures 6) Accidental release measures 7) Handling and storage 8) Exposure controls/personal protection 9) Physical and chemical properties 10) Stability and reactivity 11) Toxicological information 12) Ecological information 13) Disposal considerations 14) Transport information 15) Regulatory information 16) Other information

Question 3

What is in SDS Section 1?

Answer 3

Product identification, supplier details, emergency contact

Question 4

What is in SDS Section 2?

Answer 4

Hazards identification (GHS classification, label elements, other hazards)

Question 5

What is in SDS Section 4?

Answer 5

First aid measures (symptoms, immediate care steps)

Question 6

What is in SDS Section 5?

Answer 6

Firefighting measures (extinguishing media, hazards, PPE for firefighters)

Question 7

What is in SDS Section 9?

Answer 7

Physical and chemical properties (appearance, pH, boiling/melting point, flash point, solubility)

Question 8

What is in SDS Section 14?

Answer 8

Transport information (UN number, proper shipping name, hazard class, packaging group)

Question 9

What is different in Finland’s cosmetic regulation compared to the EU?

Answer 9

Finland requires national poison centre notification in addition to EU regulations

Question 10

Which countries follow EU cosmetics regulation?

Answer 10

EU Member States + EEA countries: Iceland, Liechtenstein, Norway

Question 11

Which products are NOT classified as cosmetics?

Answer 11

Animal shampoo, disinfectants, insect repellents

Question 12

When did the EU ban on animal testing for final cosmetic products enter into force?

Answer 12

2013

Question 13

What is CNPN?

Answer 13

Cosmetic Product Notification Portal – online system for EU cosmetic notifications

Question 14

Who must register products in CNPN?

Answer 14

Responsible person placing the product on the EU market

Question 15

Who is considered the responsible person for cosmetics?

Answer 15

Manufacturer or importer in the EU

Question 16

Who needs a PIF (Product Information File)?

Answer 16

The responsible person for the cosmetic product

Question 17

What is included in the PIF?

Answer 17

Qualitative and quantitative formula, safety assessment, GMP, animal testing data, product description

Question 18

What is the Candidate List in REACH?

Answer 18

List of Substances of Very High Concern (SVHCs)

Question 19

Where are substances requiring authorization listed?

Answer 19

REACH Annex XIV

Question 20

Where are substance restrictions listed?

Answer 20

REACH Annex XVII

Question 21

Who must register a substance under REACH?

Answer 21

Manufacturers or importers in the EU producing/importing >1 ton/year

Question 22

Which substances are exempt from REACH registration?

Answer 22

Polymers, non-isolated intermediates, substances used in medicinal products, food, cosmetics

Question 23

What is an SVHC?

Answer 23

Substance of Very High Concern (e.g. CMR, PBT, vPvB)

Question 24

Which authorities can issue environmental permits in Finland?

Answer 24

AVI (Regional State Administrative Agencies), municipal environmental authorities

Question 25

What are the functions of ELY?

Answer 25

Monitor environmental status, protect water systems, suggest measures for improvement

Question 26

What does ELY stand for?

Answer 26

Centre for Economic Development, Transport and the Environment

Question 27

When can additional maternity leave be granted under OHS?

Answer 27

If risks from CMR substances at the workplace cannot be eliminated

Question 28

What does the Act on Young Employees regulate?

Answer 28

Working hours, tasks, and protections for employees under 18

Question 29

What is a biological binding value?

Answer 29

Concentration of a chemical or metabolite in blood or urine that indicates exposure

Question 30

What is the goal of OHS legislation?

Answer 30

Protect workers' health and safety in the workplace

Question 31

Which REACH annex contains restrictions?

Answer 31

Annex XVII

Question 32

Which REACH annex contains substances requiring authorization?

Answer 32

Annex XIV

Question 33

Who can propose a restriction?

Answer 33

Member States or ECHA (at Commission’s request)

Question 34

Who can initiate an authorization process?

Answer 34

European Commission or ECHA

Question 35

Who must register substances under REACH?

Answer 35

Manufacturers/importers in the EU; non-EU entities cannot register

Question 36

Which other regulations place restrictions on substances?

Answer 36

Sector-specific laws, POP Regulation (Persistent Organic Pollutants), RoHS

Question 37

What is an Exposure Scenario?

Answer 37

Document describing how to safely use a substance, including operational conditions and risk management measures

Question 38

Who needs an Exposure Scenario?

Answer 38

Manufacturers/importers of hazardous substances >10 t/year

Question 39

What is included in an Exposure Scenario?

Answer 39

Uses, operational conditions, risk management measures, exposure estimation

Question 40

When must an Exposure Scenario be attached to a SDS?

Answer 40

When the substance is registered >10 t/year and is hazardous

Question 41

What is toxicology?

Answer 41

The study of harmful effects of chemicals on humans and other organisms

Question 42

What factors influence toxicity?

Answer 42

Dose, exposure time, route of exposure, individual sensitivity, chemical properties

Question 43

What are common routes of exposure in toxicology?

Answer 43

Inhalation, ingestion, dermal contact

Question 44

What is LD50?

Answer 44

Dose at which 50% of test animals die – indicates acute toxicity

Question 45

What does OHS stand for?

Answer 45

Occupational Health and Safety

Question 46

What does GLP stand for?

Answer 46

Good Laboratory Practice

Question 47

What does ISO stand for?

Answer 47

International Organization for Standardization

Question 48

What does IPR stand for?

Answer 48

Intellectual Property Rights

Question 49

What does ECHA stand for?

Answer 49

European Chemicals Agency

Question 50

What does PBT stand for?

Answer 50

Persistent, Bioaccumulative, and Toxic

Question 51

What does vPvB stand for?

Answer 51

Very Persistent and Very Bioaccumulative

Question 52

What does CLP stand for?

Answer 52

Classification, Labelling and Packaging

Question 53

What does GMO stand for?

Answer 53

Genetically Modified Organism

Question 54

What does GHS stand for?

Answer 54

Globally Harmonized System

Question 55

What does CRM stand for?

Answer 55

Carcinogenic, Reproductive Toxicant, Mutagenic

Question 56

What organisms are used for systemic exposure testing in ecotoxicology?

Answer 56

Algae, Daphnia, fish

Question 57

What is a product retailer?

Answer 57

An entity that sells the product to end users (not necessarily the manufacturer)

Question 58

Which products are exempt from REACH registration?

Answer 58

Polymers, non-isolated intermediates, certain natural substances, substances in food and medicines