CONTRACT

This contract is made effective as on September 3, 2016, by and between

AA Pharmaceuticals Contract Acceptor and AMAS PHARMA
Contract Giver, With reference to notification S.R.O. 412 (1) 2014,
DRAP (Drug Regulatory Authority of Pakistan), Ministry of National Health
Services Regulations and Coordination, Government of Pakistan.

1. PURPOSE OF CONTRACT: The written agreement which is

accepted between the Contract Acceptor And Contract
Giver, specifying their respective responsibilities relating to
the manufacture and control of the products.
a. According to the S.R.O. 412 (1) 2014. Rule # 02 (Xvi).
AA Pharmaceuticals Contract Acceptor is the
Manufacturer of Alternative Medicines.
All technical aspects of this contract are drawn up by
the competent person who is knowledgeable in
pharmaceutical technology, analysis and Good
Manufacturing Practice (GMP)
All arrangements for manufacture and analysis will be in
accordance with the marketing authorization and
agreed by both parties.
All batches been manufactured by Contract
Acceptor will be ensured from the Qualified Person,
and will be checked for compliance with the
requirements of Marketing Authorization.
All materials, relating to the products for manufacturing
for Contract Giver will be sole responsibility of
Contract Acceptor. Also Contract Acceptor will
be responsible for testing and releasing materials,
undertaking production and quality controls, including
in-process controls, and also for sampling and analysis.

All manufacturing, analytical and distribution records,

and reference samples will be kept by, or will be
available to, the Contract Giver. Any records
relevant to assessing the quality of a product in the
event

of complaints or a suspected defect must be accessible

and specified in the defect or recall procedures of the
Contract Giver.
The Contract Giver will be permitted to visit the
facilities of the Contract Acceptor. But it will be
subject to inspection by the competent Authorities.

CONTRACT ACCEPTOR RESPONSIBILITIES:

A. According to the S.R.O 412 (1) Rule # 02 (XV), Contract
Acceptor is having adequate premises and equipment,
knowledge & experience, and competent personnel to carry
out satisfactorily the work ordered by the Contract Giver.
B. According to the S.R.O 412 (1) Rule # 02 (XV), Contract
Acceptor will ensure that all products or materials delivered
to Contract Giver are suitable for their intended purpose.
C. According to the S.R.O 412 (1) Rule # 02 (XV), Contract
Acceptor will not pass to a third party any of the work
entrusted to him under the contract without the Contract
Givers prior evaluation and approval of the Arrangements.
D. According to the S.R.O 412 (1) Rule # 02 (XV), Contract
Acceptor will refrain from any activity which may adversely
affect the quality of the product manufactured or analyzed for
the Contract Giver.

CONTRACT GIVER RESPONSIBILITIES:

A. According to the S.R.O 412 (1) Rule # 02 (XVII), Contract
Giver will assess the competence of the Contract Acceptor
that they are carrying out successfully the work required and

also will ensure that the principles and guidelines of GMP are
followed.
B. According to the S.R.O 412 (1) Rule # 02 (XVII), Contract
Giver will provide the Contract Acceptor with all the
necessary information to carry out the

contracted operation correctly in accordance with marketing

authorization and any other legal requirements.
C. According to the S.R.O 412 (1) Rule # 02 (XVII), Contract
Giver will ensure that the Contract Acceptor is fully aware
of any problems associated with the product or the work
which might pose a hazard to his premises, equipment,
personnel, other materials or other products.
D. According to the S.R.O 412 (1) Rule # 02 (XVII), Contract
Giver will ensure that all processed products delivered by the
Contract Acceptor comply with their specifications or that
the products have been released by a Qualified Person.

AA PHARMACEUTICALS, the Contract Acceptor agrees to produce the

products (List attached) for Amas PharmaContract Giver in the quantity,
price and all other specifications determined in this agreement.
b. ORDERS & PAYMENTS: All orders should accompany a
Cheque or D.D in the name of AA Pharmaceuticals 50%
advance and the rest of 50% amount upon delivery of Goods.
CREDIT FACILITY will be highly discouraged.
c. DELIVERY: Time is of the essence in the performance of this
contract. For 1st order, Delivery shall be completed within six
weeks. In routine, Goods shall be delivered within Three
Weeks. Ensure that you have received the stocks according to
the quantities printed. Inform immediately if any Deviation
observed.

d. STOCK INVENTORY: State of inventory Four weeks initially,

later Six weeks level for each product at all times.
e. ARBITRATION: Any controversies or disputes arising out of or
relating to this contract shall be resolved by binding
arbitration in accordance with the current Commercial
Arbitration Act. The parties shall select a mutually

Acceptable arbitrator knowledgeable about the issues relating

to the subject matter of this contract.
f. CONFIDENTIALITY: Upon termination of this contract, AA
Pharmaceuticals Contract Acceptor will return to Amas
Pharma Contract Giver all records, notes, documentation
and other items that were used, created or controlled during
this contract.
g. NOTICE: Both parties have right to terminate the contract
agreement by serving Three months notice.
h. ENTIRE CONTRACT: This contract contains the entire
agreement of the parties regarding the subject matter of this
contract and there are no other promises or conditions in any
other agreement whether oral or written, this contract
supersedes and prior written or oral agreements between the
parties.
i. AMENDMENT: This contract may be modified or amended if
the amendment is made in writing and signed by both parties.

AA PHARMACEUTICALS will be responsible for matters relating to

Health Department, Manufacturing and The Quality Assurance
as well as quality control are the sole responsibility of TheA A
Pharmaceuticalsonly.
InformA A Pharmaceuticalsimmediately (within Three days) about
any complaints regarding the quantity of the shipper / product. Delay
or failure to inform promptly will not be entertained by AA
PHARMACEUTICALS.

The above mentioned products manufactured by AA

PHARMACEUTICALS, are only for the Pakistan Market. The product is
the right of Amas Pharma in all cases and supporting material /
documentation is to be provided by AA Pharmaceuticals in case of an
Export opportunity arises at no extra cost or delay of time. But all
expenses related to Export, will be sole responsibility of Amas
Pharma.
In case of occurrence of any dispute, it will be settled in Faisalabad
Court.

Marketing / Sales of the supplied products will be sole responsibility

of Amas Pharma.AA Pharmaceuticals will not share any marketing
cost, and supplies will be made on Non-Refundable basis.
For printing materials, the manufacturer name will be AA
Pharmaceuticals and marketed by or a product of Amas Pharma.
Any change in the manufacturing process or the shape of the product
will be communicated well in advance by AA Pharmaceuticals to Amas
Pharma.
The size, shape and colour scheme, design and informative material of
the product, is the sole responsibility of the Amas Pharma.
The SOPs and specifications will be provided by AA Pharmaceuticals
whenever needed to Amas Pharma.
The storage facility for the Glorious Pharmaceuticals (Semi
Finished products) may be extended by AA Pharmaceutical son
request of Amas Pharma.
The AA Pharmaceuticals has no right to supply directly or indirectly
Amas Pharma products to any institution or local Pakistani market
and any other country.
The AA Pharmaceuticals will provide brand warranty of each batch to
Amas Pharma.

If above terms and conditions are acceptable, please sign the duplicate
copy of this contract and return us as a token of acceptance.

Mr. SHAHZAD

Mr. SAJJAD
MUNAWAR
HUSSAIN HASHMI

C.E.O.
AA PHARMACEUTICALS
Faisalabad.

C.E.O.
AMAS PHARMA
Faisalabad.

Witness 1:________________
2:_______________

Witness