|
|






Based on the target date, we will prepare a master plan with a proposed timeline. |


Based on the equipment selected, our experts will prepare a set of SOPs for initial and periodic calbration and operation of all instruments. |


Based on the location of your company, our partner-agency will find key senior personnel for your company, and our experts will train them. |


all rights reserved to EHL Pharma, LLC- 2005 |
How Our Companies Can Work Together |
EHL Pharma LLC |
Generic Pharmaceutical Start-Up Specialist |
Copyright 2005 EHL Pharma, LLC |
STEP 1 |
Our experts will identify your company's needs. |
STEP 2 |
STEP 3 |
Based on your company's needs and our expertise, we will prepare an equipment selection list. |
STEP 4 |
We will minimize your expenses by avoiding the purchase of unnecessary equipment. |
STEP 5 |
Based on your company's structure, our experts will prepare a set of operation SOPs. |
STEP 6 |
STEP 7 |
We can develop and validate your first group of products and submit your first group of ANDAs. |
RESULTS |
After 3 months, your company can operate an analytical and product development laboratory that is properly validated, fully equipped, staffed with trained key personnel and has the necessary set of SOPs and other documentation. After 6 months, your company can have a manufacturing department that is properly validated, fully equipped, staffed with trained key personnel and has the necessary set of SOPs and other documentation. Furthermore, your company will be supported by a properly organized and trained Quality Assurance department. After 9 months, your company can submit to the FDA its first two ANDAs and have a properly organized and trained Regulatory Affairs department. After 12 months, your company can start manufacturing and distribution of its first three OTC products. |