MESO-Rx

Anabolic Steroids

olympianpharma.ltd - US Domestic

ve79 said:
Lol I love this community. I'm a new member and I love to see we protect each other from bullshit
Click to expand...
These days is a walk in the park for new sources… I have understood old vets would tear them a new one… like this guy clearly having another lab
 
Olympian Pharmaceutical said:

1. Verify our Peptides​

  • HPLC Analysis: we confirm the peptide’s purity (ideally above 95% pure).

2. Prepare Injectable Formulation​

  • Dissolve the Peptide: we dissolve the purified peptide into our injectable oils, GSO or MCT our two available variations on our website
  • Adjust pH & Osmolarity: we confirm the solution is at the right pH (usually pH 4-7) and is isotonic with the body (around 300 mOsm/L).
  • Sterilize: we use PPES-Series High Purity Pharmaceutical Grade Polyethersulfone Filter cartridges to tripple filter the solution and remove bacteria using a sterile filter (0.22 microns).
  • Preservatives: we then add preservatives like benzyl alcohol if needed to prevent bacterial growth.

3. Packaging ​

  • Vial Filling: we transfer the peptide solution into sterile vials.
  • Labeling: we then label with the solution name, concentration, and expiration date as well as batch number from our testing facility Janosjik Labs

4. Storage​

  • Temperature: we store our solutions in a cool, dry environment this helps prevent degradation and maintains potency.
  • Light Protection: we keep the solutions away from light, as UV exposure can degrade the solution
  • Humidity Control: for dry peptides we store in an airtight container to avoid moisture, which could compromise the solution (dry solutions)

5. added measures
  • as added sterility measures, we ensure all surfaces are constantly cleaned while paying attention to keep all solutions separate to avoid any sort of possible cross contamination
  • air filters are in place all around our lab to also ensure microscopic impurities have less chance of finding their way into the solutions prior to the filtering process
  • all items that must be handle by hand are done so using proper equipment from the begging of the process to the end we do our best to make sure there is no contamination
Click to expand...
I’m a teacher. I know chat gpt when I see it. lol
 
Bump. Answer or remove "pharmaceutical grade" from your intro and website.

readalot

Post in thread 'olympianpharma.ltd - US Domestic'

Pharma COA for finished oil:

503B Outsourcing Facility COA:

All I see are HPLC test results. Where's the rest of your testing results?

1.HPLC purity? [Done]

2. Sterility?

3. Endotoxins?

4.GCMS organic/structural impurities?

5.Metals?

6. GCMS residual solvents?

1 through 3 would put you close to a compounder who is sourcing raws from API supplier. The rest gets you to big pharma.

Feel free to share your...
  • Like
  • Love
 
Olympian Pharmaceutical said:

1. Verify our Peptides​

  • HPLC Analysis: we confirm the peptide’s purity (ideally above 95% pure).

2. Prepare Injectable Formulation​

  • Dissolve the Peptide: we dissolve the purified peptide into our injectable oils, GSO or MCT our two available variations on our website
  • Adjust pH & Osmolarity: we confirm the solution is at the right pH (usually pH 4-7) and is isotonic with the body (around 300 mOsm/L).
  • Sterilize: we use PPES-Series High Purity Pharmaceutical Grade Polyethersulfone Filter cartridges to tripple filter the solution and remove bacteria using a sterile filter (0.22 microns).
  • Preservatives: we then add preservatives like benzyl alcohol if needed to prevent bacterial growth.

3. Packaging ​

  • Vial Filling: we transfer the peptide solution into sterile vials.
  • Labeling: we then label with the solution name, concentration, and expiration date as well as batch number from our testing facility Janosjik Labs

4. Storage​

  • Temperature: we store our solutions in a cool, dry environment this helps prevent degradation and maintains potency.
  • Light Protection: we keep the solutions away from light, as UV exposure can degrade the solution
  • Humidity Control: for dry peptides we store in an airtight container to avoid moisture, which could compromise the solution (dry solutions)

5. added measures
  • as added sterility measures, we ensure all surfaces are constantly cleaned while paying attention to keep all solutions separate to avoid any sort of possible cross contamination
  • air filters are in place all around our lab to also ensure microscopic impurities have less chance of finding their way into the solutions prior to the filtering process
  • all items that must be handle by hand are done so using proper equipment from the begging of the process to the end we do our best to make sure there is no contamination
Click to expand...



I just used chatgpt for
"preparation of injectable formulations for safety sterility"

You can see how they used the outline (incase it wasn't obvious already), deleted some things, changed some words around and mentioned specific things in the same order.

pretty much the opposite of what you want to do to have random strangers trust you, seeing a lot of these types of sources





ChatGPT said:​


The preparation of injectable formulations for safety and sterility is a highly controlled process that requires strict adherence to guidelines to minimize the risk of infection, contamination, and other safety concerns. Below is a detailed overview of the key steps involved in the preparation of injectable formulations to ensure safety, sterility, and overall quality:

1.​

  • Peptide or Active Ingredient: The primary compound (e.g., peptide, drug) must be of high purity and sourced from reputable manufacturers.
  • Solvents and Carriers: Commonly used solvents include sterile water, saline, or oils (such as GSO, MCT oil) depending on the chemical properties of the active ingredient.
  • Preservatives: If the formulation is to be stored for multiple uses, preservatives such as benzyl alcohol, phenol, or others may be added to prevent bacterial growth.
  • Buffers: To ensure the stability of the active ingredient, buffer agents (e.g., phosphate, citrate) may be included to adjust the pH of the solution to an optimal level (usually pH 4–7).

2.​

  • Lyophilized Peptides: If the peptide or drug comes in a lyophilized (freeze-dried) form, it will need to be reconstituted. The reconstitution should be done with a sterile solvent like bacteriostatic water or saline.
  • Solvent Selection: Use the solvent recommended by the manufacturer or a compatible one to ensure the stability of the compound and avoid any potential reactions with the active ingredient.

3.​

  • pH Adjustment: Most injectable formulations require a specific pH range for stability and to prevent irritation upon injection. Typically, pH ranges from 4 to 7, depending on the type of compound. pH meters and buffers are used to carefully adjust the pH.
  • Osmolarity: The osmolarity of the solution must be adjusted to ensure it is isotonic with the human body (around 300 mOsm/L). If the solution is too concentrated or too diluted, it can cause irritation or other adverse effects at the injection site.

4.​

  • Sterility Requirements: Injectable formulations must be sterile to prevent infections and complications.
  • Filtration: A commonly used method for ensuring sterility is filtration through a 0.22-micron sterile filter. This is effective in removing bacteria and other microbial contaminants.
    • Polyethersulfone (PES) Filters: Pharmaceutical-grade filters, such as PPES-Series High Purity Pharmaceutical Grade Polyethersulfone, are used to filter the solution.
    • Triple Filtration: Triple filtering may be done to ensure the solution is free from bacteria, endotoxins, and particulates. The filtration process should be conducted under aseptic conditions.
  • Autoclaving: In some cases, autoclaving (steam sterilization) is used to sterilize both the solution and packaging, but this method can be unsuitable for heat-sensitive compounds like peptides.

5.​

  • Preservatives: Some injectable formulations require the addition of preservatives to prevent microbial growth, especially when the product will be used multiple times (e.g., in multi-dose vials).
    • Benzyl Alcohol: This is a commonly used preservative in injectable formulations, particularly for longer-term storage and multi-dose applications. It helps inhibit bacterial growth without affecting the integrity of the peptide or drug.
    • Other Preservatives: Depending on the formulation, other preservatives like phenol, chlorobutanol, or thimerosal may be used.
  • Final Sterility Testing: Before the final release, the formulation should undergo sterility testing, such as the USP <71> sterility test, to confirm that the product is free of microbial contamination.

6.​

  • Packaging: Injectable formulations should be packaged in sterile, airtight containers or vials. Glass vials are typically preferred, though certain types of plastic vials may also be used if they meet pharmaceutical standards.
  • Sealing: After filling the vial, it should be sealed with a sterile rubber stopper and crimped with an aluminum cap to maintain sterility during storage.
  • Storage: The storage conditions should be followed based on the type of formulation:
    • Cold Storage: Many injectable formulations, especially peptides, should be stored in a refrigerator (2–8°C) to maintain their stability.
    • Room Temperature: Some formulations may be stored at room temperature but must be protected from light and heat.

7.​

  • Visual Inspection: Every vial of injectable formulation should be visually inspected for any particulate matter, discoloration, or signs of contamination.
  • Endotoxin Testing: If required, endotoxin testing (e.g., Limulus Amebocyte Lysate (LAL) test) should be performed to ensure that the formulation is free from harmful endotoxins, which can cause severe reactions when injected.
  • Potency Testing: The potency of the final product should be tested to ensure that the active ingredient remains within the intended concentration range.

8.​

  • Throughout the entire process, aseptic technique must be strictly followed. This includes wearing gloves, using sterile equipment, and working in a clean, controlled environment, such as a laminar flow hood or clean room.

9.​

  • Each batch should be properly labeled with relevant information, such as:
    • Drug or peptide name and concentration
    • Lot number
    • Expiration date
    • Storage instructions
  • Detailed records of each step in the preparation process should be maintained for quality control and traceability.
 
Liter O' Test said:
I just used chatgpt for
"preparation of injectable formulations for safety sterility"

You can see how they used the outline (incase it wasn't obvious already), deleted some things, changed some words around and mentioned specific things in the same order.

pretty much the opposite of what you want to do to have random strangers trust you, seeing a lot of these types of sources





ChatGPT said:​


The preparation of injectable formulations for safety and sterility is a highly controlled process that requires strict adherence to guidelines to minimize the risk of infection, contamination, and other safety concerns. Below is a detailed overview of the key steps involved in the preparation of injectable formulations to ensure safety, sterility, and overall quality:

1.​

  • Peptide or Active Ingredient: The primary compound (e.g., peptide, drug) must be of high purity and sourced from reputable manufacturers.
  • Solvents and Carriers: Commonly used solvents include sterile water, saline, or oils (such as GSO, MCT oil) depending on the chemical properties of the active ingredient.
  • Preservatives: If the formulation is to be stored for multiple uses, preservatives such as benzyl alcohol, phenol, or others may be added to prevent bacterial growth.
  • Buffers: To ensure the stability of the active ingredient, buffer agents (e.g., phosphate, citrate) may be included to adjust the pH of the solution to an optimal level (usually pH 4–7).

2.​

  • Lyophilized Peptides: If the peptide or drug comes in a lyophilized (freeze-dried) form, it will need to be reconstituted. The reconstitution should be done with a sterile solvent like bacteriostatic water or saline.
  • Solvent Selection: Use the solvent recommended by the manufacturer or a compatible one to ensure the stability of the compound and avoid any potential reactions with the active ingredient.

3.​

  • pH Adjustment: Most injectable formulations require a specific pH range for stability and to prevent irritation upon injection. Typically, pH ranges from 4 to 7, depending on the type of compound. pH meters and buffers are used to carefully adjust the pH.
  • Osmolarity: The osmolarity of the solution must be adjusted to ensure it is isotonic with the human body (around 300 mOsm/L). If the solution is too concentrated or too diluted, it can cause irritation or other adverse effects at the injection site.

4.​

  • Sterility Requirements: Injectable formulations must be sterile to prevent infections and complications.
  • Filtration: A commonly used method for ensuring sterility is filtration through a 0.22-micron sterile filter. This is effective in removing bacteria and other microbial contaminants.
    • Polyethersulfone (PES) Filters: Pharmaceutical-grade filters, such as PPES-Series High Purity Pharmaceutical Grade Polyethersulfone, are used to filter the solution.
    • Triple Filtration: Triple filtering may be done to ensure the solution is free from bacteria, endotoxins, and particulates. The filtration process should be conducted under aseptic conditions.
  • Autoclaving: In some cases, autoclaving (steam sterilization) is used to sterilize both the solution and packaging, but this method can be unsuitable for heat-sensitive compounds like peptides.

5.​

  • Preservatives: Some injectable formulations require the addition of preservatives to prevent microbial growth, especially when the product will be used multiple times (e.g., in multi-dose vials).
    • Benzyl Alcohol: This is a commonly used preservative in injectable formulations, particularly for longer-term storage and multi-dose applications. It helps inhibit bacterial growth without affecting the integrity of the peptide or drug.
    • Other Preservatives: Depending on the formulation, other preservatives like phenol, chlorobutanol, or thimerosal may be used.
  • Final Sterility Testing: Before the final release, the formulation should undergo sterility testing, such as the USP <71> sterility test, to confirm that the product is free of microbial contamination.

6.​

  • Packaging: Injectable formulations should be packaged in sterile, airtight containers or vials. Glass vials are typically preferred, though certain types of plastic vials may also be used if they meet pharmaceutical standards.
  • Sealing: After filling the vial, it should be sealed with a sterile rubber stopper and crimped with an aluminum cap to maintain sterility during storage.
  • Storage: The storage conditions should be followed based on the type of formulation:
    • Cold Storage: Many injectable formulations, especially peptides, should be stored in a refrigerator (2–8°C) to maintain their stability.
    • Room Temperature: Some formulations may be stored at room temperature but must be protected from light and heat.

7.​

  • Visual Inspection: Every vial of injectable formulation should be visually inspected for any particulate matter, discoloration, or signs of contamination.
  • Endotoxin Testing: If required, endotoxin testing (e.g., Limulus Amebocyte Lysate (LAL) test) should be performed to ensure that the formulation is free from harmful endotoxins, which can cause severe reactions when injected.
  • Potency Testing: The potency of the final product should be tested to ensure that the active ingredient remains within the intended concentration range.

8.​

  • Throughout the entire process, aseptic technique must be strictly followed. This includes wearing gloves, using sterile equipment, and working in a clean, controlled environment, such as a laminar flow hood or clean room.

9.​

  • Each batch should be properly labeled with relevant information, such as:
    • Drug or peptide name and concentration
    • Lot number
    • Expiration date
    • Storage instructions
  • Detailed records of each step in the preparation process should be maintained for quality control and traceability.
Click to expand...
This guy is a class act… don’t even entertain this shit bruv… he is clearly muscle candy or axle rebranded…
 
Spam: repeatedly copy/paste same message
FastBun said:
This guy is a class act… don’t even entertain this shit bruv… he is clearly muscle candy or axle rebranded…
Click to expand...
we are not here to argue with accusations about our company, if Youd like to take advantage of our November sale there's plenty of time left. if not thanks for stopping by! we carefully consider each comment thanks for the support!
 
Hi, I’m here for some to buy some olypian gear.
I heard labels are pretty cool and have exclusive Easter eggs sometimes, such as a quirky misspelling of the compound ordered. For example, instead of test its tren, or maybe trest. I’m fucking excited for my mystery blast!! I’d like some more info please, waiting to hear from you Mr olip man.
 
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