SDS (Safety Data Sheets) Records - When and how long?

G

Griff23

Hello Everyone and Happy Friday,

I'm setting up a HazCom program and starting to prepare for going BS 18001 certified. I'm having a problem finding the information on when and for what do we need to keep SDS's records.

We only have 4 chemicals we purchase and keep on site to sell or use in assembly. Gear oil and hose lubricants (water based, env. friendly).

What about other substances like WD-40, lithium grease, etc.? (all quanities under a quart)

How do you handle lets say if engineering brought into the facility a pint of lubricant to test with?

And how long do you keep SDS's records?

Any help or a point in the right direction of were to locate this information would be great. I have found some information on the OSHA websites but no specific info. on quantities or what is excluded from having to keep records.

Thank you
Griff23
 
M

mguilbert

I do not believe there is any quantity limit. A drop of some chemicals can be very dangerous. I am no expert but I think you would need MSDS for all chemical agents in case someone gets some in their eyes or skin.
 

Randy

Super Moderator
29CFR 1910.1200 will tell you everything you need to know as well as the guidance you'll find on the OSHA website.
 

Henria

OSH Officer
Hi !

Yes indeed you must comply with the OSH regulations of your country, but OSH regulations are the basis for the occupational risks pr?vention, not the end.

Whatever quantity and duration of using a substance or mixture the chemical OSH procedure must be the same: the SDS and the proposed method of use should be the basis for risk assessment of the project (simple test or industrial process ...).

What will change depending of the size of a chemical project is the size of the preventive provisions we decide, more or less important, strong or durable ...

Then (even for a simple test) it is useless to archive this "experience" (the SDS and the using caracteristiks). You can use these datas if a similar projet later appears or if legal problems then arise for example).

Bye.
 

Jen Kirley

Quality and Auditing Expert
Leader
Admin
When reviewing requirements under 29CFR 1910.1200 it's important to understand the difference between manufacturer and user.

As per 1910.1200(b)(4)(ii), if you obtain chemicals for use at your site, even temporarily or on a trial basis, people who could be exposed to the chemicals need to have access to the information a Safety Dada Sheet provides "during each shift" and 1910.1200(b)(4)(iii) directs you to provide employee training on the program. It makes sense to only keep up-to-date SDSs for currently used chemicals immediately available, but you should keep a history file of everything for research purposes. Keeping them current shouldn't be difficult because I see very little changes in MSDS over time, but I suggest a periodic review of these documents of external origin anyway.

If you only have a small number of such chemicals, I would keep it simple and just post a binder with them in an area where employees on each shift can have easy access. Some people use stations and binders like this commercially available example, but that's not needed as long as everyone who might need to read the SDSs know where they are, can access them on their shift (I would put one in their work area or some place easy to get to but hard to get lost) and understand how to use them. Keep it simple.

It's important that everyone who would be obtaining a chemical is involved with your HAZCOM process in that they tell you of their plans, ideally before they purchase the stuff so you can avoid getting something really nasty if a more friendly alternative is available. Again, keep it simple.

29 CFR 1910.1200 doesn't talk about records.

I hope this helps!
 
Last edited:

Randy

Super Moderator
Under 1910.1020, the MSDS is considered a record and as per 1910.1020(d)(1)(ii)(B), "need not be retained for any specified period as long as some record of the identity (chemical name if known) of the substance or agent, where it was used, and when it was used is retained for at least thirty (30) years...."

Trust me, if someone is brave enough to play silly games with OSHA they can toss the old MSDS's (or SDS as they are now known). The easiest way to retain information about chemicals used in the workplace is the MSDS.

Records for safety and environmental go way, way beyond what might be expected, especially when you could wind up in the defendants chair.
 

Mikishots

Trusted Information Resource
Hello Everyone and Happy Friday,

I'm setting up a HazCom program and starting to prepare for going BS 18001 certified. I'm having a problem finding the information on when and for what do we need to keep SDS's records.

We only have 4 chemicals we purchase and keep on site to sell or use in assembly. Gear oil and hose lubricants (water based, env. friendly).

What about other substances like WD-40, lithium grease, etc.? (all quanities under a quart)

How do you handle lets say if engineering brought into the facility a pint of lubricant to test with?

And how long do you keep SDS's records?

Any help or a point in the right direction of were to locate this information would be great. I have found some information on the OSHA websites but no specific info. on quantities or what is excluded from having to keep records.

Thank you
Griff23

I'm in Canada, and these rules are clearly spelled out in our OHS laws.

Where I work, Engineering is not permitted to bring in ANY controlled product without it going through Receiving. Receiving is to ensure that an MSDS has been provided by the manufacturer before accepting the shipment. If there isn't one, the courier has to remove it from the premises.

If a controlled product is on the premises, an MSDS sheet no older than three years must be made available.

Doesn't matter if the product is environmentally friendly, water-based, or under a quart - if it meets the definition of a controlled product, you need an MSDS. BTW, WD-40 is highly flammable and is mildly toxic (aspiration hazard).

Here in Canada, the six classes of controlled products are:

Class A - Compressed Gas
Class B - Flammable and Combustible Material
Division 1: Flammable Gas
Division 2: Flammable Liquid
Division 3: Combustible Liquid
Division 4: Flammable Solid
Division 5: Flammable Aerosol
Division 6: Reactive Flammable Material
Class C - Oxidizing Material
Class D - Poisonous and Infectious Material
Division 1: Materials causing immediate and serious toxic effects
Subdivision A: Very toxic material
Subdivision B: Toxic material
Division 2: Materials causing other toxic effects
Subdivision A: Very toxic material
Subdivision B: Toxic material
Division 3: Biohazardous Infection Material
Class E - Corrosive material
Class F - Dangerously reactive material
 
K

kgott

I cant speak for any other jurisdiction but In Australia an MSDS or SDS as they are referred to these days must be immediately available for the user and emergency services to consult. This means they have to be in close proximity to the substance.

MSDS's must be renewed every 5 years as manufactures can change the formulation of the substance and therefore the physical and chemical properties of the substance which may affect reactivity, toxicity and other relevant characteristics.

The SDS is used as the basis for the risk assessment, handling, storage, safe use, identification of PPE etc. A risk assessment must be carried out on each substance.

The employer must have an SDS for each and every chemical. For example, for petrol (gas in the US) they must have a SDS for each brand and each type. The MSDS for unleaded petrol is different to that for super grade.

One oil company's petrol is different to another oil company's petrol and therefore they have to have an MSDS for each brand and type. All petrols have the same UN number but you cannot just have an SDS for the UN number alone.

If anyone is looking for software to manage chemicals with Chemalert is a very popular program in Australia, you buy an annual subscription and the program works of Chemalert servers.

Risk assessments can be done in Chemalert

[FONT=&quot]RMT - Chemalert[/FONT]
[FONT=&quot]www.rmt.com.au/chemalert.htm[/FONT]
[FONT=&quot]Used by over 1000 clients across 6000 sites worldwide, ChemAlert continues to set the benchmark in chemical safety management systems. [/FONT]

I have nothing to do with the company at all but their product is very good. I use it here and I've used in other work places

cheers
 
Last edited by a moderator:

Henria

OSH Officer
Hello !

Kgott, I don't completly agree with you regarding two point :

- I am not ok to say "MSDS's must be renewed every 5 years" because there is no "periodicity" for the validity of a SDS. For the user to wait 5 years to verify if a FDS is still valid seems too long for me. Especially as normally if the supplier updates a SDS he must notify his to its customers (provide the new version).

- To carry out risk assessment "on each substance" is not very relevant. For risks assessement it's imperative to analyse the processtoo ! So if I have still assessed risks of a first process using le substance ou mixture A, a second different process with the same chemical A needs to do a second risk assessment ! So the target of chemical risk assessment is not the chemicals but the couples "chemical + process". So I say "A risk assessment must be carried out on each substance-process". "Chemical A + process 1" is different of "chemical A + process 2" and "Chemical A + process 1" is different of "chemical B + process 1". I think this approach is very important.

Bye.
 
Thread starter Similar threads Forum Replies Date
S Examples of FDA acceptable Software Design Specification (SDS) Medical Device and FDA Regulations and Standards News 6
6 Management of SDS and Hazardous Material Occupational Health & Safety Management Standards 2
R GHS compliance - Are we are required to provide an SDS? Manufacturing and Related Processes 5
D SDS (MSDS) for complex products such as a TV, computer, cars, etc Miscellaneous Environmental Standards and EMS Related Discussions 3
I Any Recommendations on (M)SDS Databases or Services? Occupational Health & Safety Management Standards 4
sagai What if ... Source code part of the SDS (Software Design Specification) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 13
S Recruitment Industry Service Delivery Standard (RCSA-SDS) - getting started Various Other Specifications, Standards, and related Requirements 3
P EN 62304 Safety Class of an ECG device designed to be used in clinical situations when patient is in immediate danger. IEC 62304 - Medical Device Software Life Cycle Processes 3
R Regarding safety requirements of the Lid latch mechanism CE Marking (Conformité Européene) / CB Scheme 1
D FDA combo product-need to define direct & indirect impact regarding safety,quality & regulatory.Can anyone point me in right direction-SupplierMgmt 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
E QMS references in Safety Assurance Case? US Food and Drug Administration (FDA) 4
F Safety program The Reading Room 1
J Determination of software safety class (62304) prior to software risk analysis ISO 14971 - Medical Device Risk Management 3
M Software Safety Classification and Legacy Software IEC 62304 - Medical Device Software Life Cycle Processes 4
A Safety testing of Medical devices ISO 13485:2016 - Medical Device Quality Management Systems 2
A Safety testing for Medical devices to be sold in India ISO 13485:2016 - Medical Device Quality Management Systems 0
Q Where to place our Safety Program in our QMS? Occupational Health & Safety Management Standards 9
Q Safety Training Program Training - Internal, External, Online and Distance Learning 8
T Book Excerpt: Drugs and the FDA: Safety, Efficacy, and the Public’s Trust Book, Video, Blog and Web Site Reviews and Recommendations 0
M Safety assessment of cosmetic product EU Medical Device Regulations 1
H EMC & Safety Testing of the product with the same Sr. No. for EC Declaration CE Marking (Conformité Européene) / CB Scheme 3
A Quality and Safety in one. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
D ISO 14001 Finding - Missing Safety Data Sheets ISO 14001:2015 Specific Discussions 2
V Functional safety for Fuses and Fuse boxes ISO 26262 - Road vehicles – Functional safety 0
armani Monitoring and measuring equipment for occupational health and safety purposes Occupational Health & Safety Management Standards 10
T Testing for proving food safety on USP class vi material RoHS, REACH, ELV, IMDS and Restricted Substances 0
T Internal and external communication procedure for Food Safety Food Safety - ISO 22000, HACCP (21 CFR 120) 2
H Product Safety & Conformity Representative (PSCR) Training Company IATF 16949 - Automotive Quality Systems Standard 0
T FDA level of concern vs IEC 62304 safety classification - 510(k) exempt device Other US Medical Device Regulations 13
S Safety testing IEC 60601 series Medical Device and FDA Regulations and Standards News 2
K Electrical Safety Tester ISO 13485:2016 - Medical Device Quality Management Systems 7
H Harmonized Standard for the refrigerated lab device safety CE Marking (Conformité Européene) / CB Scheme 2
H Regarding the validity of EMC & Safety test reports without NABL & ILAC-MRA mark. CE Marking (Conformité Européene) / CB Scheme 2
H Regarding EMC & Safety retesting requirements of the product CE Marking (Conformité Européene) / CB Scheme 2
L Article 87 Field Safety Corrective Actions in a third country EU Medical Device Regulations 2
S Risk control through Information for safety ISO 14971 - Medical Device Risk Management 12
Ron Rompen 4.4.1.2 Product Safety Compliance IATF 16949 - Automotive Quality Systems Standard 30
B QMS Functional Safety Checklist ISO 26262 - Road vehicles – Functional safety 0
H Characteristics related to safety - format of documentation ISO 14971 - Medical Device Risk Management 3
Watchcat Raising new questions of safety and effectiveness Other US Medical Device Regulations 4
Anerol C In Charge of Safety - New- Safety program Example Occupational Health & Safety Management Standards 6
Aymaneh Summary of safety and performance (SSP) IVDR 2017/746 EU Medical Device Regulations 1
S Summary of safety and clinical performance and Article 120(3) of the MDR EU Medical Device Regulations 4
Sidney Vianna Food & Beverage Safety Lead Auditor Open Position - USA Job Openings, Consulting and Employment Opportunities 0
D ISO 26262 functional safety : how to get started Other ISO and International Standards and European Regulations 8
A What is different between Field Safety Notice and Advisory Notice in U.S and EU? Document Control Systems, Procedures, Forms and Templates 7
A TGA - Annual Report or Periodic Safety Update Report? Other Medical Device Regulations World-Wide 0
B IVDR Electrical safety standard EU Medical Device Regulations 0
Z Choice of PTC heater voltage to maximize user safety and ease of CE compliance to LVD CE Marking (Conformité Européene) / CB Scheme 0
M Post Market Safety Update Report for devices that will be up-classified under MDR but are currently under MDD EU Medical Device Regulations 6

Similar threads

Top Bottom