How to Read UN Packaging Codes

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The basis of all national and international regulations for the safe transport of dangerous goods are the Recommendations ("Specification") of the "UN Committee of Experts" as published in "The Orange Book".


There are five different (relevant) Modal Authorities who each publish their own regulation manuals in which they follow "The Orange Book".

These are the:
The Technical Instructions for the Safe Transport of Dangerous Goods by Air published by the International Civil Aviation Authority (ICAO).


The International Maritime Dangerous Goods Code (IMDG) published by the International Maritime Organisation (IMO).


The European Agreement concerning the International Carriage of Dangerous Goods by Road (ADR) published by The United Nations Economic Commission for Europe (UNECE).


The International Agreement for the Carriage of Dangerous Goods by Rail (RID) published by The Intergovermental Organisation for International Carriage by Rail (OTIF).


The Hazardous Materials Regulations (Title 49 CFR Parts 100-185) published by The Office of Hazardous Materials Safety, US DOT.


What are Dangerous Goods?

Goods which are classified as dangerous for transport range from those which are highly dangerous (such as explosives and fuming acids) to everyday products such as paints, solvents and pesticides found in the home and at work. Dangerous goods, which can also be called "Hazardous Materials" (mainly in the US), may be substances or products. The transport of such goods is regulated to ensure the safety of life, of the ship, aircraft or vehicle, and of other goods (such as foodstuffs) being transported. For example, solvents must be in sealed airtight containers otherwise the fumes could affect people in the close vicinity. Other substances may not be harmful unless they come into contact with fire or water, but for safety purposes these are also classified as dangerous goods.

When transporting "Hazardous Materials", in most cases, the packaging has to be certified to UN standards. The international agreements for the carriage of dangerous goods require packaging to be of a design-type certified by a national competent authority. This involves testing the packaging against the appropriate UN specification to ensure its suitability for the carriage of certain dangerous goods. Such packaging is often referred to as "type-approved", "UN Approved" or "UN certified" and marked in a particular way, prefixed by the UN logo and followed by codes.

The UN Marking System

The U.N. marking system indicates several characteristics of the packaging, as well as information on the test levels the packaging has successfully passed. Because these test levels are related to the hazard level and physical and chemical characteristics of the substance to be filled, the markings also indicate some of the properties of the materials that may be packed in each container.

A sample UN Marking:
1H2 / Y1.8 / 100 / 08 / F / OA30900


UN The United Nations Coding System


1
Type of Container
1. Drums/Pails
2. Barrels
3. Jerricans
4. Boxes
5. Bags
6. Composite Packagings


H
Material of Construction
A. Steel
B. Aluminum
C. Wood
D. Fibre
E. Plastic


2
Category Within Type
1. Closedhead
2. Openhead


Y
Packaging Group for which container was tested
X. for Packaging Group I, II, III
Y. for Packaging Group II and III
Z. for Packaging Group III
Packaging Group I: Great Danger - high hazard levelPackaging Group II: Medium Danger - medium hazard levelPackaging Group III: Minor Danger - low hazard level


1.8
Density or specific gravity of material packedORFor packaging intended for Solids (powders, pills, capsules, tablets) or that have inner packaging, this marking will indicate the maximum gross mass (weight) in kilograms.


100
Hydraulic pressure in kilo-pascal (kPa)ORFor packaging intended for Solids or that have inner packaging, an "S" in upper case will follow the gross mass.


08
Current year


F
Country where container was manufactured


OA30900
Code for manufacturing plant

Part-Time Courses for Regulatory Affairs, Quality control and Quality Assurance in Mumbai

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What is Regulatory Affairs?
Regulatory Affairs (RA) is an upcoming profession within the biomedical / health products sector. RA profession at its heart is all about Collecting, Analyzing and Communicating the Risks and Benefits of health care products to regulatory agencies and public all over the world.

In an organization their prime responsibilities involves preparation and presentation of registration documents to regulatory agencies and carry out all following discussion to obtain and maintain marketing authorization (MA) for the products concerned.

They need to keep a track on ever changing legislation in all countries where the companies is looking to market their product.

RA profession is broader than registration of products, they advise companies both strategically and technically at the highest level. Their role begins right from development of a product to making, marketing and post marketing. Their advice at all stages both in terms of legal and technical requirements and restrains help companies save a lot of time and money in developing the product and marketing the same.

They have a major contribution in company’s success both Commercially and Scientifically.

Careers in Regulatory Affairs:-
Pharma is a highly regulated industry the world over and professionals, who can manage regulatory affairs, are in high demand.

Selling drugs is not like selling anything else, when we sell drugs we need to be confident that
They do what they claim to do They have been through a tough testing process to get from the lab to the market The side effects are well documented.

This is where regulatory affairs come in.

“Regulatory Affairs Professional is the key link to distributing your drugs to world region.”

The Indian Pharmaceutical industry is one of the fastest growing industry in India, with a CAGR of over 13 % in last 5 years and it is expected to grow at a higher rate in coming 10 years. It is valued at $ 8.0 billion approximately and ranks 4th in terms of volume and 13th in terms of value globally.

With such a high growth rate and rapid globalization there is a substantial need for highly trained professionals ready to perform the work required within this specialized industrial sector who will keep updates with regulatory law, policies and procedures for one or more product lines as well as maintain an understanding of the scientific and technical background of new products.
The increasing graph of the global companies’ setup in India demands the trained and skilled professional on a Handsome Salary, looking back for past few years rise in salary is multiplying.
There is a widening gap of rising demand and too few skilled human resource, this has seen a 50 % zoom on average in salaries for skilled manpower specifically in CRO sector alone. On an average there has been over 30% rises in salaries in Pharmaceutical Sector.

Research & Development activity in the Pharma sector is seeing a rapid growth and this growth is only poised to increase the need for skilled manpower and higher pay scale to retain the skilled.

What you will need to become a RA professional :-
A good background knowledge of the pharmaceuticals and medical environment A meticulous approach to work.Attention to detail.

Academic Qualification in Regulatory Affairs
You can expect to work in a multidisciplinary workplace where scientists and medics will come from very different backgrounds. Excellent written and verbal communication skills are a must as is the ability to work effectively under pressure.

It is not easy for any Science Graduate to get a good salary hike in the pharmaceutical/chemical industry without having the appropriate qualification/knowledge. However, when a person spends at least 2-3 years in the same field, he/she can master the job. However, to be a project leader or to get into the higher ranks of the organization, a person needs to be aaware of the changing trends of the industry. This is where Regulatory Affairs plays an important role. With environmental issues cropping up each day and the stringent measures adopted by Environmental Protection agencies, FAO and the WHO and other NGOs, it is very important for an organization to have an individual who can flexibly handle and understand all the critical procedures of the company and can help in the amooth functioning of the company.
For all Life Science Graduates or Basic Science Graduates working in Pharmaceuticals /Agrochemicals companies, can enhance their knowledge and have an edge over your peers by having any additional Diploma or Certificate courses.

Some of the institutes offering courses on the same lines through Part-time for working professionals or Through distance Education are:
Institute of Pharmaceutical Management - (IPM), Dombivli.
Global Institute of Regulatory Affairs, Pune.
Bioinformatics Institute of India, Noida.

UN Packing Group for Pesticides/Agrochemicals

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AGROCHEMICALS PACKING GROUPS
ALPHA-CYPERMETHRIN. III
CYPERMETHRIN III
ACEPHATE II
ACETAMIPRID III
ALUMINIUM PHOSPHIDE I
BIFENTHRIN III
BUPROFEZIN III
CARBARYL III
CARTAP HYDROCHLORIDE III
CHLORPYRIFOS III
DELTAMETHRIN II & III
DIAZINON III
DICHLORVOS II & III
DICOFOL II & III
DIMETHOATE III
ENDOSULFAN II
ETHION II
CARBENDAZIM III
COPPER OXYCHLORIDE III
HEXACONAZOLE II & III
MANCOZEB III
METALAXYL III
PROPICONAZOLE III
PROPINEB II & III
ANILOPHOS II
ATRAZINE III
BPMC III
BUTACHLOR III
CLODINAFOP-PROPARGYL III
2,4-D SODIUM SALT III
2,4 D DIMETHYL AMINE SALT III
2,4-D ETHYL ESTER II & III
FENOXAPROP-P-ETHYL III
GLYPHOSATE III
CARBENDAZIM + MANCOZEB III
CHLORPYRIFOS + CYPERMETHRIN III
QUINALPHOS + CYPERMETHRIN I & III
DELTAMETHRIN + TRIAZOPHOS II & III
ALPHA NAPHTHYL ACETIC ACID II & III
AMINO ACID III
BACILLUS THURINGIENSIS N/A
UREA III
MICRONUTRIENTS N/A
FIPRONIL III
FENVALERATE III
IMIDACLOPRID III
INDOXACARB III
LAMBDA-CYHALOTHRIN III
MALATHION III
METHYL PARATHION II
MONOCROTOPHOS II
OXYDEMETON-METHYL III
PERMETHRIN III
PHOSPHAMIDON II
PROFENOFOS III
QUINALPHOS I & II
TEMEPHOS III
THIAMETHOXAM II & III
TRIAZOPHOS III
ZINC PHOSPHIDE I
SULFUR III
THIOPHANATE METHYL III
THIRAM III
TRICYCLAZOLE II
VALIDAMYCIN III
ZIRAM I & III
IMAZETHAPYR III
ISOPROTURON III
METRIBUZIN III
OXYFLUORFEN 95 % II
OXYFLUORFEN 24 % III
PARAQUAT DICHLORIDE II
PENDIMETHALIN III
PRETILACHLOR III
SULFOSULFURON III
METSULFURON METHYL III
TRICLOPYR III
STREPTOMYCIN + TETRACYCLINE II
MANCOZEB + METALAXYL III
PROFENOPHOS + CYPERMETHRIN III
ETHION + CYPERMETHRIN II & III
ETHION II
BENTONITE SULPHUR PASTILLES III
ETHEPHON III
GIBBERELLIC ACID III
Note: Packing Group/Class for all pesticides/ fungicides/ herbicides/ weedicides/ insecticides (Agrochemicals) varies with Different formulations.
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