MESO-Rx Sponsor Genuine Steroid Powder Manufacturer-AASraw

Thanks for your question.

Every product has its specification and standard when it comes out. And the standard is different with different products. We manufacture the products based on pharma standards and make ingredient analysis for each batch. And we also make certificate of analysis and HPLC report at the same time. Until confirmation the products meet standards, we sell them in market. Impurity analysis is part of our routine QC program. We only analyze if the impurity is within standard, like 0.5%, 0.1%. As for what the impurity is, it needs separate analysis by specialized machines.

Here is a certificate of analysis for Tadalafil, it shows the standard. And impurities are within limits.
Thank you for your response. So your company goes to the trouble of putting together a USP like C of A but then doesn't go to the trouble of posting them? Why aren't you giving yourself credit for the work performed?

Thank you for the C of A provided. I asked for results from some of your AAS raws. For example, post C of A for a batch of your (1) test cyp and (2) oxandrone raws. Specifically note the assays used for each of the impurity checks (purity, impurity, metals, RS, etc). That way users here get a solid education on what to look for and can indepently verify your results with 3rd party lab.

Why aren't you testing for all elemental impurities instead of just heavy metals?

Why aren't you doing standard residual solvents (RS) assay? Are only those solvents listed because those are the only ones used in the process? Look up the USP reporting options for elemental impurities and residual solvents.

Appreciate your time and you should share all the work to help your business and support verification by 3rd party analysis. Would put you far ahead of competition. Very far.
 
What happened to AASraw.com? Disappeared?
Official response: No! AASraw is now also called Aea Ltd.


We are thrilled to share that AASraw (now called Aea.ltd.) has recently undergone a major server upgrade to enhance your experience. In any case, our dedication to quality and innovation remains steadfast.

View attachment AEA.webp
 
So what is different about AASraw/Aea.ltd now?

1. Stable and Reliable Quality:

Aea.ltd./AASraw has passed ISO 9001:2015 quality system certification. All the products are strictly manufactured according to cGMP standards and match pharmaceutical grade.
• Quality control covers all aspects, including in-process quality control, batch analysis, warehouse labeling, release control, and batch sample storage.

2. Enhanced R&D Capabilities:
• Advanced process R&D and a specialized pilot plant in Shanghai Juke Biotech Park for rapid developments and early-phase API manufacturing.
• Dedicated to drug research and development, our upgraded facilities in Shanghai boast reactors ranging from 50L to 3000L, supporting custom synthesis of almost any organic compound. We specialize in intermediates, reference compounds, and derivatives of lead compounds
• Our company is equipped with HPLC, GC, and other analytical instruments. Tests can be done on IR, GC/MS, LC/MS, and 400NMR at the SIOC through contract.Once the projects come into our R&D center, our highly experienced chemists will conduct a quick initial evaluation. From first batch sample submission to pilot scale-up and chemistry validation, we emphasize speed without compromising quality.

3. Delivery Capabilities Improvement:
• A state-of-the-art commercial production site in Hangzhou Gulf Fine Chemical Zone, equipped with state-of-the-art facilities, is capable of handling from grams to multi-hundred-metric-ton operations. Ensuring flexibility and reliable lead times for our customers.
We appreciate your continued trust and look forward to delivering unparalleled services in the pharmaceutical field.
Thank you for your continued support of the AASraw/AEA Ltd. company.
For further information, please contact us Email: King@aea.ltd
 
So what is different about AASraw/Aea.ltd now?

1. Stable and Reliable Quality:

Aea.ltd./AASraw has passed ISO 9001:2015 quality system certification. All the products are strictly manufactured according to cGMP standards and match pharmaceutical grade.
• Quality control covers all aspects, including in-process quality control, batch analysis, warehouse labeling, release control, and batch sample storage.

2. Enhanced R&D Capabilities:
• Advanced process R&D and a specialized pilot plant in Shanghai Juke Biotech Park for rapid developments and early-phase API manufacturing.
• Dedicated to drug research and development, our upgraded facilities in Shanghai boast reactors ranging from 50L to 3000L, supporting custom synthesis of almost any organic compound. We specialize in intermediates, reference compounds, and derivatives of lead compounds
• Our company is equipped with HPLC, GC, and other analytical instruments. Tests can be done on IR, GC/MS, LC/MS, and 400NMR at the SIOC through contract.Once the projects come into our R&D center, our highly experienced chemists will conduct a quick initial evaluation. From first batch sample submission to pilot scale-up and chemistry validation, we emphasize speed without compromising quality.

3. Delivery Capabilities Improvement:
• A state-of-the-art commercial production site in Hangzhou Gulf Fine Chemical Zone, equipped with state-of-the-art facilities, is capable of handling from grams to multi-hundred-metric-ton operations. Ensuring flexibility and reliable lead times for our customers.
We appreciate your continued trust and look forward to delivering unparalleled services in the pharmaceutical field.
Thank you for your continued support of the AASraw/AEA Ltd. company.
For further information, please contact us Email: King@aea.ltd
Good day Fellows, I ordered 2 different raw compounds from AASraw. It took 21 days to reach me in Canada.
 
Thank you for your response. So your company goes to the trouble of putting together a USP like C of A but then doesn't go to the trouble of posting them? Why aren't you giving yourself credit for the work performed?

Thank you for the C of A provided. I asked for results from some of your AAS raws. For example, post C of A for a batch of your (1) test cyp and (2) oxandrone raws. Specifically note the assays used for each of the impurity checks (purity, impurity, metals, RS, etc). That way users here get a solid education on what to look for and can indepently verify your results with 3rd party lab.

Why aren't you testing for all elemental impurities instead of just heavy metals?

Why aren't you doing standard residual solvents (RS) assay? Are only those solvents listed because those are the only ones used in the process? Look up the USP reporting options for elemental impurities and residual solvents.

Appreciate your time and you should share all the work to help your business and support verification by 3rd party analysis. Would put you far ahead of competition. Very far.
And please don't post anymore HPLC results based on area count only. Please assess purity in am accurate way (detected mass of AAS in raw using calibrated HPLC / mass sample).

The proper method requires relative response factor for API using a reference standard.

Thank you.
Thank you for your sincere suggestions and recognition of our quality culture. It can be seen that you have researched a lot about testing of products.

1. We make certificate of analysis but didn't make a post for each batch because the quality is stable and the test result is almost same. When some customers ask for it in ordering, we will share with them COA of that batch product.

2. We don't analyze all elemental impurities and standard residual solvents assay because we confirm that they are within limits and it is not an easy process, which will cost too many sources. But if customer has requirements when discussing a specific order, our lab will make an analysis based on his needs.

3. HPLC is one of the results in several test ways. We also make HNMR, MS tests, especially for CMO and CDMO products.

I will feedback it to our technical team and consider your suggestions seriously! Thank you again!
 
Good day Fellows, I ordered 2 different raw compounds from AASraw. It took 21 days to reach me in Canada.
Thanks for your sharing. Looking forward to further cooperation! Hope we can bring better shipping to you in the future.
 
Sure my pleasure.
We don't analyze all elemental impurities and standard residual solvents assay because we confirm that they are within limits and it is not an easy process, which will cost too many sources
So you intermittently test your raws for elemental impurities and residual solvents?

What is the mean +/- SD (range) weight percent impurity levels on your AAS raws?

Can you describe what those impurities consist of?

Example...
1% side product / raw material
0.25% elemental impurities
1.5% residual solvent

Can you comment if your residual solvent QC approach adheres to USP <467> option 1 or 2?

Thanks!
 
Sure my pleasure.

So you intermittently test your raws for elemental impurities and residual solvents?

What is the mean +/- SD (range) weight percent impurity levels on your AAS raws?

Can you describe what those impurities consist of?

Example...
1% side product / raw material
0.25% elemental impurities
1.5% residual solvent

Can you comment if your residual solvent QC approach adheres to USP <467> option 1 or 2?

Thanks!
The percentage of impurities is different in different AAS. Most impurities are androstadienedione and synthetic intermediate testosterone.

Our residual solvent QC approach adheres to USP <467> option 2.
 
Holiday Reminder

Our office and factory will be closed from 2th Feb. to 18th Feb. 2024 for the Chinese Spring Festival.

Please feel free to contact us with any questions on holiday.

Email: King@aea.ltd

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The percentage of impurities is different in different AAS. Most impurities are androstadienedione and synthetic intermediate testosterone.

Our residual solvent QC approach adheres to USP <467> option 2.
Thank you for your reply. So what is the mean +/- SD purity for the AAS raws you offer? That should give the user a good summary of the breakdown unless you have a few purities that skew the distribution.

Option 2 huh? Interesting. In that case what are the typical residual solvents and their calculated daily exposure values? What components are exceeding Option 1 limits (since you are using Option 2)?
 
Notification
We are officially back to work from Spring Festival holiday. Products are in stock and can be shipped out soon. Any inquiry are welcome; pls feel free to talk!

Website: www.aea.ltd

Email: King@aea.ltd
 
HGH Test Report

A customer sent our HGH to Janoshik lab last month. The test result is 97.2%.

HGH-Janoshik-20240127.png
 
I have two Jano blind tests that I would share
Results are very good
 

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