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About Venapro Hemorrhoids Relief Treatment
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Venapro manufactures and distributes Venapro hemorrhoids relief treatment along with a wide variety of
herbal supplements, liquid formulas, and capsule products. We create unique,
safe and effective products that help people supplement their lives.
Venapro has formulated a unique and highly effective line of herbal
dietary supplements. It is our goal to provide retailers and vendors with
the finest quality supplements ever made at wholesale prices barely above
our manufacturing costs. We are proud to offer a wide range of 'high demand'
herbal supplements made only from the finest pharmaceutical grade
ingredients available.
For over 15 years, Venapro has been committed to helping our customers,
large and small, gain and maintain a competitive edge in the herbal
supplements marketplace.
We offer private labeling upon request and committed to helping our
customers, large and small, gain and maintain a competitive edge in the
herbal supplements marketplace. Wholesale Inquiries
CLICK HERE
All of our raw materials must pass stringent quality controls before they
are utilized. In addition, we use only those precursor materials that are of
the highest quality that pass our in house quality inspection.
Quality Control
All raw materials are tested for purity prior to production. Quality control
engineers have the authority to reject any product during any stage of
production that does not adhere to our strict quality standards. All
personnel follow explicit written protocols that are strictly enforced
during the manufacturing process. All steps during the manufacturing process
are documented and reviewed by quality control specialist. Manufacturing
equipment is properly maintained and cleaned on a predetermined schedule
which is documented in company logs for review by the Department of
Agriculture. This helps to ensure the absence of any contamination during
the manufacturing process. Production records associated with each unit of a
product including all raw materials used are filed for two years past the
expiration date.
Further quality control is demonstrated in the following manner:
Product analysis - is recorded for each product that is manufactured. This
analysis contains the specific components of the herbal product including a
lot number for each of the ingredients and the productions methods used.
Raw materials - are purchased only from reputable wholesalers. Each raw
material in our products must come with a Certificate of Analysis provided
obtained from the supplier. Our in house quality assurance team also
analyzes the raw materials for authenticity.
Packaging material - all packaging materials are purchased only from
reputable wholesalers. Specific quality assurance personal ensure that all
labels are assigned to the proper products manufactured to avoid any
confusion. All new labels are cross checked with the original master label
to ensure there has been no mistakes during the printing process.
Lot Numbers - once an order request has been received the herbal supplement
to be manufactured is entered in the production records and a lot number is
assigned. The raw materials are subsequently released to the pharmacy once
all products have been checked for authenticity.
Venapro Manufacturing Guidelines
In addition to the above outlined protocols for the physical aspect of the
manufacturing facility. Venapro Supplements also adheres to the
following manufacturing guidelines to ensure the utmost quality control:
Blending and Granulation - all equipment used for in the process of mixing
and granulation are inspected by the director of operations prior to use.
Raw materials are then inspected for the final time and the lots are then
processed using the strict written guidelines for each herbal product.
Following granulation and blending the powder blends are stored in
specifically designed containers to ensure freshness and to avoid any
contamination. Once again the director of operations ensures that all new
blends are labeled appropriately.
Encapsulation and Compression ? all equipment used for in the process of
mixing and granulation are inspected by the director of operations prior to
use. Raw materials are then inspected for the final time and the lots are
then processed using the strict written guidelines for each herbal product.
Once a test unit has been processed a sample is unit is issued to quality
assurance to be compared to retained samples insure product integrity. Once
the new unit has been approved by quality assurance the full line production
may begin. Quality assurance inspections are conducted using set protocols
for the capsules. As with the blending and granulation process the capsules
are stored in specifically designed containers to ensure freshness and to
avoid any contamination. The director of operations ensures that all new
capsules are labeled appropriately.
Liquids - follow the same stringent protocol as the the above mentioned
blending, granulation, encapsulation and compression procedures.
Packaging and Inspection - upon completion of the processing, the final
product is inspected again by the quality control staff, broken tablets,
over filled capsules, and other defective finished products are removed from
the lot. Products released by the quality control staff are subsequently
either packaged for bulk storage or bottled and labeled for consumer use
(labels contain the appropriate information as required by the Federal Drug
Administration, batch numbers are logged). All finished products are
properly labeled and closed with a tamper proof seal. The quality control
unit also retains samples of raw materials (for one year past the expiration
date of the last product they are used in) and finished products (for one
year past the product expiration date) are maintained under control
conditions. All of our liquid products follow the same stringent control
standards were applicable.
Final Products - all final products are stored in quarantine in a climate
controlled environment until final delivery to the customer.
All of Venapro Supplements are manufactured using Good Manufacturing
Practices set forth by the US Federal Drug Administration. In addition, both
scheduled and surprise inspections by the quality control staff during
different aspects of the manufacturing process help to ensure specific
quality, strength and purity for both the raw materials and the finished
supplements. |
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